Desde la Federación Ben Magec Ecologistas en Acción, que agrupa a colectivos de todas las islas, manifestamos nuestra enorme preocupación por la situación de las compañeras de la Plataforma Canarias se Agota que llevan ya 14 días en huelga de hambre, con alto riesgo para sus vidas, reivindicando otro modelo de turismo para Canarias. La entrada Ben Magec Ecologistas en Acción muestra su apoyo y preocupación por los compañeros de ‘Canarias se Agota’ en huelga de hambre hace catorce días aparece primero en Ecologistas en Acción.
On April 10, a delegation of European Entrepreneurs joined our French Member M-ETI on a day of meetings with the highest institutions of France. The post European Entrepreneurs & European Family Business discuss with French Senate and National Assembly the needs and challenges for the European Mittelstand appeared first on European Entrepreneurs CEA-PME.
La directora de '20.000 especies de abejas', ganadora de 3 premios Goya y nominada al Premio del Público LUX del Parlamento Europeo, ha destacado en numerosas ocasiones que su película es, en cierto modo, un homenaje a Ekai, un joven trans que, antes de quitarse la vida, pidió que su caso sirviese para dar visbilidad. La película, no solo da voz a la realidad de las infancias trans, sino que también aborda el papel y las limitaciones de las etiquetas. En esta entrevista, la directora explora el poder del cine para "comprender el dolor humano desde un lugar más íntimo, que otro tipo de acercamientos no nos permiten".
La directora de '20.000 especies de abejas', ganadora de 3 premios Goya y nominada al Premio del Público LUX del Parlamento Europeo, ha destacado en numerosas ocasiones que su película es, en cierto modo, un homenaje a Ekai, un joven trans que, antes de quitarse la vida, pidió que su caso sirviese para dar visbilidad. La película, no solo da voz a la realidad de las infancias trans, sino que también aborda el papel y las limitaciones de las etiquetas. En esta entrevista, la directora explora el poder del cine para "comprender el dolor humano desde un lugar más íntimo, que otro tipo de acercamientos no nos permiten".
In a world where financial data abounds, leveraging this information can propel a business to new heights. Anastasija Tenca, Chief Operations Officer at Noda, sheds light on the transformative power of open banking in harnessing this data for business growth. As the financial landscape evolves, Noda's innovative solutions are leading the charge in turning data […]
The Academy is a full and active member of the ESDC and is the course director of one of the most important cyber courses on the ESDC’s ETEE platform, ‘The The post On 13 March 2024, the European Security and Defence College (ESDC) hosted a delegation from the Italian Interagency Law Enforcement Academy of Advanced Studies (Department of Public Security) at the ESDC’s headquarter in Brussels. appeared first on ESDC- European Security & Defence College.
Hoy, dos metodologías han sido aprobadas por la Comisión, una destinada a medir la cantidad de microplásticos en el agua y, otra que garantiza la reutilización de las aguas residuales utilizadas en el riego agrícola. También tienen el objetivo de reforzar la calidad y resistencia del agua en toda la UE.
Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the safety and efficacy of monensin sodium (Coxidin®) as a coccidiostat for chickens for fattening, chickens reared for laying, turkeys for fattening and turkeys reared for breeding. The additive currently on the market complies with the existing conditions of authorisation. The FEEDAP Panel concluded that Coxidin® remains safe for turkeys for fattening (up to 16 weeks) and extends this conclusion to turkeys reared for breeding (up to 16 weeks). The Panel was not in the position to confirm that the current maximum authorised level of 125 mg monensin sodium/kg complete feed remains safe for chickens for fattening and chickens reared for laying. The use of monensin sodium from Coxidin® at the corresponding maximum authorised/proposed use levels in the target species is safe for the consumer. The existing maximum residue levels (MRLs) for poultry tissues ensure consumer safety. No withdrawal time is necessary. Both formulations of Coxidin® pose a risk by inhalation. The formulation with wheat bran as a carrier was neither irritant to the skin nor a skin sensitiser but it was irritant to the eyes. In the absence of data, no conclusions could be made on the potential of the formulation containing calcium carbonate to be irritant to skin and eyes and to be a skin sensitiser. The use of monensin sodium from Coxidin® in complete feed for the target species poses no risk for the terrestrial compartments and for sediment. No risk for groundwater is expected. For chickens for fattening the risk for aquatic compartment cannot be excluded, but no risks are expected for the other animal categories. There is no risk of secondary poisoning. Coxidin® is efficacious in controlling coccidiosis at a level of 100 mg/kg complete feed for chickens for fattening and at 60 mg/kg complete feed for turkeys for fattening. These conclusions are extended to chickens reared for laying and turkeys reared for breeding. The Panel noted that there are signs of development of resistance of Eimeria spp. to monensin sodium.
Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the safety and efficacy of Enterococcus lactis DSM 22502 as a technological feed additive for all animal species. The applicant provided evidence that the additive currently on the market complies with the existing conditions of authorisation. There is no new evidence that would lead the FEEDAP Panel to reconsider its previous conclusions regarding the safety and efficacy of the additive. The FEEDAP Panel concluded that E. lactis remains safe for all animal species, consumers and environment under the authorised conditions of use. Regarding the user safety, the Panel concluded that the additive is not irritating to the skin or eyes. No conclusions can be drawn on the potential of the additive to cause skin sensitisation, but it is considered to be a respiratory sensitiser. There is no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.
EIB Global, part of the European Investment Bank, and the Housing Finance Bank (HFB) of Uganda have announced a partnership to avail €50 million investment to support private sector entities, notably SMEs in Uganda.
564128 Željka Šulc From 3 to 6 March 2024, the OSCE Mission to Bosnia and Herzegovina (BiH) organized a study visit for representatives of the BiH Central Election Commission to the Central Election Commission of Albania. This visit provides insights into the application of election technologies and electoral processes. Albania has successfully integrated new election technologies into its systems for number of years. Ilirjan Celibashi, State Election Commissioner of the Republic of Albania, emphasized the importance of increased communication and exchange of good practices. "The study visit of our Bosnian and Herzegovinian colleagues presents an opportunity to foster regional communication and connect the Election Commission of Albania with other Election Commissions in the region. Regional cooperation is vital to address common challenges and ensure mutual support. Therefore, establishing a regular platform for the exchange of information and experiences can foster a robust and professional network." Irena Hadžiabdić, President of the BiH Central Election Commission, said: "Amidst discussions on electoral reform and the upcoming pilot project for the use of electoral technologies in the next elections, the experiences of other countries, particularly the lessons learned from Albania, are invaluable. We extend our sincere gratitude to the OSCE Mission to BiH and the Election Commission of Albania for organizing this study visit." The study visits to the Central Electoral Commission of Albania featured presentations on the experiences of electoral implementation bodies and other institutions involved in the political/legislative processes preceding the pilot project implementation. Topics included procurement modalities, staff training, data transfer, cyber security, and other issues pertaining to the introduction of election technologies “As we navigate the complexities of electoral processes, it's imperative that we remain open to learning from the experiences of others. By drawing insights from diverse perspectives, we can fortify our efforts towards meaningful election reform,” said Ahmed Rifatbegović, National Political Officer at the OSCE Mission to BiH. “Embracing reform not only strengthens the integrity of our democratic institutions but also reinforces public trust in the electoral system.” Participants also had the opportunity to share experiences with representatives from the Central Election Commission, the Agency for the Protection of Personal Data and the Agency for Identification Documents, Records and Data Exchange. This study visit is part of the OSCE Mission to BiH's broader project, "Improving the Integrity of Electoral Processes in 2024 and 2026 in accordance with the recommendations of the ODIHR and international standards." This project is implemented with the support of the Governments of the Kingdom of Norway, United Kingdom, USA, and Germany.
Call for tender - EEA/DIS/R0/23/007 - Copernicus Land Monitoring Service - Pan European Component - Production and Validation of High Resolution Vegetation Phenology and Production admin Wed, 06/03/2024 - 12:53 Procedure identifier EEA/2023/OP/0054 Submission method Electronic - Open for submission Description The subject of this call for tenders is the establishment of two framework service contracts with different economic operators covering the production (lot 1) and validation (lot 2) of the pan-European - Bio-geophysical Parameters – High Resolution Vegetation Phenology and Productivity (HR-VPP). Procedure type open Estimated total value 5125000 EUR TED publication date 30/01/2024 Lead contracting authority European Environment Agency (EEA) Main classification (CPV) 72300000 - Data services Submission terms Submissions must be sent exclusively at the address for submission given below. Submission method Electronic Address for submission Access submission Wed, 06/03/2024 - 12:00
3Rs Working Party (3RsWP) plenary meeting – Public session on the 2024 work plan, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 20 March 2024, 09:00 (CET) to 20 March 2024, 10:00 (CET)
Statement by the High Representative on behalf of the European Union on the alignment of certain third countries with Council Decision (CFSP) 2024/747 of 23 February 2024 amending Decision 2014/145/CFSP concerning restrictive measures in respect of actions undermining or threatening the territorial integrity, sovereignty and independence of Ukraine.
Statement by the High Representative on behalf of the European Union on the alignment of certain third countries with Council Decision (CFSP) 2024/746 of 23 February 2024 amending Decision 2014/512/CFSP concerning restrictive measures in view of Russia’s actions destabilising the situation in Ukraine.
Statement by the High Representative on behalf of the European Union on the alignment of certain third countries with Council Decision (CFSP) 2024/577 of 12 February 2024 amending Decision 2014/512/CFSP concerning restrictive measures in view of Russia’s actions destabilising the situation in Ukraine.
Statement by the High Representative on behalf of the European Union on the alignment of certain third countries with Council Decision (CFSP) 2024/740 of 22 February 2024 amending Decision (CFSP) 2023/891 concerning restrictive measures in view of actions destabilising the Republic of Moldova.
Statement by the High Representative on behalf of the European Union on the alignment of certain third countries with Council Decision (CFSP) 2024/633 of 19 February 2024 amending Decision (CFSP) 2022/266 concerning restrictive measures in response to the illegal recognition, occupation or annexation by the Russian Federation of certain non-government controlled areas of Ukraine.
Statement by the High Representative on behalf of the European Union on the alignment of certain third countries with Council Decision (CFSP) 2024/628 of 19 February 2024 amending Common Position 2001/931/CFSP on the application of specific measures to combat terrorism.
Eight Nitrosamine Implementation Oversight Group (NIOG) meeting and Fifth Nitrosamine Implementation Oversight Group (NIOG) – meeting with pharmaceutical industry, European Medicines Agency, Amsterdam, the Netherlands, 7 September 2022
Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on Bacillus velezensis ATCC PTA‐6737 as a zootechnical additive (functional group: gut‐flora stabiliser) in the context of the renewal of the authorisation for turkeys for fattening and turkeys reared for breeding. The applicant is also requesting to modify the target species in the current authorisations to ‘all growing poultry’, the increase of the recommended use level in chickens for fattening, chickens reared for laying and minor poultry species except minor poultry for laying from 1 × 107 to 1 × 108 CFU/kg complete feed and the compatibility of the additive with halofuginone. The applicant provided evidence that the additive currently in the market complies with the conditions of the authorisation. There was no new evidence that would lead to reconsider previous conclusions. Therefore, the FEEDAP Panel concluded that the additive remains safe for all poultry species for fattening and reared for laying/breeding, the consumers and the environment under the current authorised conditions of use. The additive is not irritant to the skin and eyes, but it should be considered a respiratory sensitiser. The Panel could not conclude on the skin sensitisation potential of the additive. The Panel concluded that the additive has a potential to be efficacious as a zootechnical additive for poultry for fattening and reared for laying/breeding under the proposed conditions of use.
Training webinar on the use of Scientific Explorer in scientific advice regulatory procedures, Online, European Medicines Agency, Amsterdam, the Netherlands, from 3 April 2024, 11:30 (CEST) to 12 April 2024, 14:00 (CEST)
563668 Officers of the Border Guard Service of the State Committee for National Security (SCNS) of the Kyrgyz Republic Chyngyz Zhanybekov Aida Almazbekova From February 26 to March 1, 2024, a training course on the 'Combatting Illicit Trafficking of Small Arms and Light Weapons (SALW), Conventional Ammunition (CA), and Explosives at the border' took place in Osh, Kyrgyz Republic, aiming to address the adverse impact of illicit trafficking on safety and security in the OSCE region. The uncontrolled spread of SALW, CA, and explosives, particularly to terrorists and criminal groups, has significantly impacted the safety of populations and the security of OSCE Participating States, increasing the intensity and duration of recent armed conflicts. The training provided Kyrgyz border guard officers with an in-depth understanding of their roles in combating illicit trafficking of SALW, ammunition, and explosives, the identification of sources and proliferation of illicit SALW, and enhanced expertise in risk management. Participants gained insights into international legal frameworks, national regulations, and effective post-seizure procedures. "This training is part of the OSCE regional approach for Central Asia in strengthening the capacities of the Border and Customs Services in detecting SALW, ammunition, and explosives at border crossing points based on international best practices," noted Nora Vanaga, Associate Project Officer at the Conflict Prevention Centre in the OSCE Secretariat. "The illicit trafficking of SALW and their proliferation across national borders affect the safety of the entire population. Border guard officers play a key role in intercepting this phenomenon as they are the first to screen persons and goods entering a country. This course was designed to build the capacity of the Border Service in combating the illicit trafficking of SALW, ammunition, and explosives, with particular attention to promoting international standards in Kyrgyzstan," shared Ewa Klimuk, Project Manager at the OSCE Programme Office in Bishkek. This course was organized within the framework of the extra-budgetary project project by the OSCE Programme Office in Bishkek (POiB) and the OSCE Conflict Prevention Centre Supporting Unit, in collaboration with experts from INTERPOL, UNODC, and the German Verification Centre. The course was conducted as part of the ExB project of the POiB entitled 'Reducing the risk of the illicit proliferation of SALW, CA, and explosives across the border of Kyrgyz Republic,' funded by the Federal Republic of Germany and the United States of America. By collaborating with international partners, the OSCE is committed to supporting the Kyrgyz Republic’s efforts in addressing transnational threats and ensuring safety and security in the broader OSCE area.
Dans le cadre du séminaire Russie Interfaces, Fabrice Balanche, maître de conférences en géographie à l'Université Lyon 2 et chercheur associé au think-tank Washington Institute, viendra présenter son dernier livre « Les leçons de la crise syrienne - L’affrontement entre l’Occident, l’Iran, la Russie et la Chine », Odile Jacob, Paris, 2024.
Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the assessment of the application for renewal of the authorisation of Cylactin® as a zootechnical feed additive for cats and dogs. The active agent of the additive is Enterococcus lactis NCIMB 10415 and the micro‐encapsulated formulation, Cylactin® LBC ME5 PET, was assessed. The applicant has provided evidence that the additive currently on the market complies with the existing conditions of authorisation. The Panel concluded that the additive remains safe for cats and dogs. Regarding user safety, the additive was not shown to be skin and eye irritant, but it should be considered a respiratory sensitiser. No conclusions can be drawn on the skin sensitisation. There is no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.
The EFSA Panel on Food Contact Materials, Enzymes and Processing Aids (CEP) assessed the safety of the recycling process CeltiPak (EU register number RECYC318), which uses the Kreyenborg IR Clean+ technology. The input material is hot caustic washed and dried poly(ethylene terephthalate) (PET) flakes originating from collected post‐consumer PET containers, for example, bottles, with no more than 5% PET from non‐food consumer applications. The flakes are heated in a continuous IR dryer (step 2) before being processed in a finisher reactor (step 3). Having examined the challenge test provided, the Panel concluded that step 2 and step 3 are critical in determining the decontamination efficiency of the process. The operating parameters to control the performance of these critical steps are temperature, air/PET ratio and residence time. It was demonstrated that this recycling process is able to ensure that the level of migration of potential unknown contaminants into food is below the conservatively modelled migration of 0.10 and 0.15 μg/kg food, derived from the exposure scenario for infants and toddlers, respectively, when such recycled PET is used at up to 100%. Therefore, the Panel concluded that the recycled PET obtained from this process is not considered to be of safety concern, when used at up to 100% for the manufacture of materials and articles for contact with all types of foodstuffs, including drinking water, for long‐term storage at room temperature or below, with or without hotfill. Articles made of this recycled PET are not intended to be used in microwave and conventional ovens and such uses are not covered by this evaluation.
Following a request from the European Commission, the EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety of microcrystalline cellulose and carboxymethyl cellulose as technological feed additives for all animal species. In its previous opinions on the safety and efficacy of the products, the FEEDAP Panel could not conclude on proper identification and characterisation as required for a feed additive. The occurrence of potential toxic impurities could also not be assessed. Based on the new data provided, the feed additives microcrystalline cellulose and carboxymethyl cellulose were properly identified and characterised and were shown to meet the specifications set for their use as food additives. Therefore, the conclusions of the safety reached in the previous opinions for microcrystalline cellulose and carboxymethyl cellulose meeting the food additive specifications apply to the microcrystalline cellulose and carboxymethyl cellulose under assessment as feed additives. The additives are considered safe for all animal species, the consumer and the environment. In the absence of data, the FEEDAP Panel is not in the position to conclude on the safety for the user.
Quarterly System Demo Q1 2024, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 26 March 2024, 09:00 (CET) to 26 March 2024, 13:30 (CET)
Following a request from the European Commission, the EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety of hydroxypropyl methyl cellulose and methyl cellulose as technological feed additives for all animal species. In its previous opinions on the safety and efficacy of the products, the FEEDAP Panel could not conclude on proper identification and characterisation as required for a feed additive. The occurrence of potential toxic impurities could also not be assessed. Based on the new data provided, the feed additives hydroxypropyl methyl cellulose and methyl cellulose were properly identified and characterised and were shown to meet the specifications set for the food additives. Therefore, the conclusions of the safety assessments reached in the previous opinions for hydroxypropyl methyl cellulose and methyl cellulose meeting the food additive specifications, apply to the hydroxypropyl methyl cellulose and methyl cellulose under assessment as feed additives. The additives are considered safe for all animal species, the consumer and the environment. In the absence of data, the FEEDAP Panel is not in the position to conclude on the safety for the user.
Statement by the High Representative on behalf of the European Union on the alignment of certain third countries with Council Decision (CFSP) 2024/421 of 29 January 2024 amending Decision 2011/72/CFSP concerning restrictive measures directed against certain persons and entities in view of the situation in Tunisia.
Statement by the High Representative on behalf of the European Union on the alignment of certain third countries with Council Decision (CFSP) 2024/422 of 29 January 2024 amending Decision 2014/512/CFSP concerning restrictive measures in view of Russia’s actions destabilising the situation in Ukraine.
Authors: Elisa Uhlig, Anna Sadzik and Mara Strenger, Sustainable Packaging Institute SPI, Albstadt-Sigmaringen University In December 2023, the EU-funded projet BioSupPack organised a workshop alongside the European Bioplastics Conference - EBC23 on the topics: “The next challenge in packaging: How to choose between different bio-based polymers? How can Life Cycle Assessments be used to [...]
The EFSA Panel on Food Contact Materials, Enzymes and Processing Aids (CEP) assessed the safety of the recycling process ENPLATER (EU register number RECYC316), which uses the Kreyenborg IR Clean+ technology. The input material is hot caustic washed and dried poly(ethylene terephthalate) (PET) flakes originating from collected post‐consumer PET containers, e.g. bottles, with no more than 5% PET from non‐food consumer applications. The flakes are heated in a continuous IR dryer (step 2) before being processed in a finisher reactor (step 3). Having examined the challenge test provided, the Panel concluded that step 2 and step 3 are critical in determining the decontamination efficiency of the process. The operating parameters to control the performance of these critical steps are temperature, air/PET ratio and residence time. It was demonstrated that this recycling process is able to ensure that the level of migration of potential unknown contaminants into food is below the conservatively modelled migration of 0.10 and 0.15 μg/kg food, derived from the exposure scenario for infants and toddlers, respectively, when such recycled PET is used at up to 100%. Therefore, the Panel concluded that the recycled PET obtained from this process is not considered to be of safety concern, when used at up to 100% for the manufacture of materials and articles for contact with all types of foodstuffs, including drinking water, for long‐term storage at room temperature or below, with or without hotfill. Articles made of this recycled PET are not intended to be used in microwave and conventional ovens and such uses are not covered by this evaluation.
The EFSA Panel on Food Contact Materials, Enzymes and Processing Aids (CEP) assessed the safety of the recycling process GTX Hanex (EU register number RECYC317), which uses the Kreyenborg IR Clean+ technology. The input material is hot caustic washed and dried poly(ethylene terephthalate) (PET) flakes originating from collected post‐consumer PET containers, e.g. bottles, with no more than 5% PET from non‐food consumer applications. The flakes are heated in a continuous IR dryer (step 2) before being processed in a finisher reactor (step 3). Having examined the challenge test provided, the Panel concluded that step 2 and step 3 are critical in determining the decontamination efficiency of the process. The operating parameters to control the performance of these critical steps are temperature, air/PET ratio and residence time. It was demonstrated that this recycling process is able to ensure that the level of migration of potential unknown contaminants into food is below the conservatively modelled migration of 0.10 and 0.15 μg/kg food, derived from the exposure scenario for infants and toddlers, respectively, when such recycled PET is used at up to 100%. Therefore, the Panel concluded that the recycled PET obtained from this process is not considered to be of safety concern, when used at up to 100% for the manufacture of materials and articles for contact with all types of foodstuffs, including drinking water, for long‐term storage at room temperature or below, with or without hotfill. Articles made of this recycled PET are not intended to be used in microwave and conventional ovens and such uses are not covered by this evaluation.
Statement by the High Representative on behalf of the European Union on the alignment of certain third countries with Council Decision (CFSP) 2024/457 of 2 February 2024 amending Decision (CFSP) 2024/254 concerning restrictive measures in view of the situation in Guatemala.
The European Parliament’s vote on Strategic Technologies for Europe Platform (STEP) represents an important first move to ensure European industry remains competitive and innovative. EuropaBio welcomes the inclusion of biotech according to the OECD definition as a strategic technology for Europe. The post Biotech recognised in regulation for Europe’s future: EuropaBio welcomes European Parliament’s vote on Strategic Technologies forEurope Platform Regulation first appeared on Europabio.
The applicant Arysta Life Science Great Britain Limited submitted a request to the competent national authority in Croatia to evaluate the confirmatory data that were identified for quizalofop‐P‐tefuryl in the framework of the maximum residue level (MRL) review under Article 12 of Regulation (EC) No 396/2005 as not available. Since Article 12 data gaps were also set for the two other quizalofop‐P variants sharing the same residue definitions for risk assessment and monitoring, EFSA included in the present assessment all quizalofop‐P variants: quizalofop‐P‐ethyl, quizalofop‐P‐tefuryl and propaquizafop. Moreover, in the application submitted to Croatia, the applicant also included a request to modify the existing MRLs for quizalofop‐P‐tefuryl in grapes, sunflower seeds and soyabeans in accordance with Article 6 of Regulation (EC) No 396/2005. To address the data gaps, new data on hydrolysis efficiency of quizalofop‐P‐tefuryl, quizalofop acid, quizalofop‐pentanoic acid and quizalofop‐P‐glycerate in different matrices of animal origin in accordance with the guidance document SANTE/2020/12830 Rev.1 were submitted, along with a validated analytical method for animal commodities. EFSA concluded that the data gap on validation of the efficiency of the extraction and hydrolysis included in the enforcement method of residues in livestock animal commodities was only fully addressed for muscle, poultry liver and eggs. Regarding plant commodities, the remaining data gaps were not addressed. EFSA also considered data gaps for quizalofop‐p‐ethyl in caraway as sufficiently addressed in the context of a previous MRL application. In general, the new information provided required a revision of the existing MRLs for several commodities of plant and animal origin. Further risk management considerations are required. Based on the risk assessment results, EFSA concluded that the short‐term and long‐term intake of residues resulting from the use of quizalofop‐P‐tefuryl according to the reported agricultural practices is unlikely to present a risk to consumer health.
Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the assessment of the application for renewal of the authorisation of Pediococcus pentosaceus DSM 23689 as a technological additive, silage additive for all animal species. The applicant has provided evidence that the additive currently on the market complies with the existing conditions of authorisation. The Panel concluded that the additive remains safe for all animal species, consumers, and the environment under the authorised conditions of use. Regarding user safety, the additive should be considered as a respiratory sensitiser. No conclusions can be drawn on the skin sensitisation, and skin and eye irritancy potential of the additive. There is no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.
Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the assessment of the application for renewal of Pediococcus pentosaceus DSM 23688, a technological additive for all animal species. The applicant has provided evidence that the additive currently on the market complies with the existing conditions of authorisation. The Panel concluded that the additive remains safe for all animal species, consumers, and the environment under the authorised conditions of use. Regarding user safety, the additive was shown not to be irritant to skin or eyes. The Panel was not in the position to conclude on skin sensitisation potential of the additive, but it is considered to be a respiratory sensitiser. There is no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.
Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the safety and efficacy of a feed additive consisting of Enterococcus lactis NCIMB 11181 (Lactiferm®) as a zootechnical additive (gut flora stabiliser) for chickens for fattening, chickens reared for laying, other poultry species for fattening or reared for laying, and ornamental birds. The additive is available in two formulations: Lactiferm WS200 and Lactiferm Basic 50. The FEEDAP Panel concluded that the use of the additive is safe for chickens for fattening or reared for laying, other poultry species for fattening or reared for laying, and ornamental birds. The Panel also concluded that the use of the feed additive is safe for consumers, and the environment. Lactiferm WS200 is not irritant to skin or eyes. Owing to the proteinaceous nature of the active agent, both formulations of the additive are considered respiratory sensitisers. It was not possible, however, to conclude on the irritancy potential for skin and eyes of the Lactiferm Basic 50 formulation or on the potential of both formulations of the additive to cause skin sensitisation. The efficacy studies submitted did not allow to draw a conclusion on the efficacy of the additive for the target species. Lactiferm® is considered compatible with the coccidiostats monensin sodium and decoquinate.
Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on Bacillus velezensis ATCC PTA‐6737 as a zootechnical additive (functional group: gut flora stabilisers) in regard to the renewal of the authorisation for weaned piglets, weaned minor porcine species, sows and minor reproductive Suidae species, and its extension of use for all Suidae. The applicant provided evidence that the additive currently in the market complies with the conditions of the authorisation. The Panel concluded that there is no new evidence that would lead it to reconsider the previous conclusions; the additive is safe for the target species, consumers and the environment under the authorised conditions of use. This conclusion also applies to the target species/categories for which a request for an extension of use is made. The Panel concluded that B. velezensis ATCC PTA‐6737 is not irritant to skin or eyes but should be considered a respiratory sensitiser due to its proteinaceous nature. No conclusions could be drawn on the skin sensitisation potential of the additive. The Panel concluded that the additive has the potential to be efficacious in all growing Suidae (suckling, weaned and fattening Suidae) at the minimum inclusion level of 1 × 107 CFU/kg of complete feed and in sows and minor reproductive Suidae species at 1 × 108 CFU/kg complete feed.
EMA and European Organisation for Research and Treatment of Cancer (EORTC) workshop: How can patient-reported outcomes (PRO) and health-related quality of life (HRQoL) data inform regulatory decisions?, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, 29 February 2024
SPOR Status Update, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 10 April 2024, 10:00 (CEST) to 10 April 2024, 12:30 (CEST)
CAN Europe welcomes this opportunity to provide input to the development of guidelines for designating renewables acceleration areas (RAAs). Our input as the attached briefing titled “Renewable Energy Planning and […] The post BRIEFING: Renewable Energy Planning and Mapping for Successful Acceleration with Nature and Communities at Its Heart: Guiding Principles for Member States appeared first on CAN Europe.
European Investment Bank President Nadia Calviño today shared with EU finance ministers an ambitious strategy to build on the strengths of the EIB Group, focus on eight core policy priorities and deploy the full potential of the institution to boost growth and social and territorial cohesion, and support Europe’s leadership in the twin green and digital transitions, as well as increasing Europe´s competitiveness, open strategic autonomy and economic security.
Une évaluation faisant autorité du groupe de la Banque européenne d’investissement (BEI) sur les obstacles à l’investissement dans l’Union européenne comprend une évaluation des investissements en faveur de la résilience au changement climatique dans les systèmes de transport. L’Europe est fortement dépendante d’une infrastructure de transport fonctionnelle. Toutefois, l’incertitude quant à l’avenir, le décalage des politiques, la nature des externalités, les horizons temporels, la rareté des informations et le manque de capacités freinent les investissements dans les infrastructures adaptées au changement climatique.
On the 21st February 2024, the Ambassador Secretary General of the Parliamentary Assembly of the Mediterranean and PAM’s Head of Administration and Protocol... The post PAM Secretary General and PAM Head of Administration and Protocol visit the EMEA offices to discuss regional cooperation in the Euro-Mediterranean and the Gulf appeared first on EMEA.
Read our press statement on the Council ignoring farmers' concerns regarding Ukraine ATMs; it is now imperative for the European Parliament to take action. The post Press statement - The Council has chosen to ignore farmers' concerns regarding Ukraine ATMs, it is now imperative for the European Parliament to take action appeared first on CEFS.
Lieu et date : le 13 et 14 juin 2024 de 09h00 à 18h00 dans l'amphithéâtre 5 de l'Inalco - Pôle des Langues et Civilisations - 65 rue des Grands Moulins, 75013 Paris.
Commission Implementing Decision (EU) 2024/581 of 16 February 2024 on the harmonised standard for accreditation of medical laboratories drafted in support of Regulation (EC) No 765/2008 of the European Parliament and of the Council
Statement by the High Representative on behalf of the European Union on the alignment of certain third countries with Council Decision (CFSP) 2024/383 of 22 January 2024 concerning restrictive measures in view of activities undermining the stability and political transition of Sudan.
Press conference following the selection of the seat of the European Authority for Anti-Money Laundering and Countering the Financing of Terrorism (AMLA) will take place on 22 February 2024.
In compliance with Article 43 of Regulation (EC) No 396/2005, EFSA received from the European Commission in 2020 a mandate to provide its reasoned opinion on the toxicological properties and maximum residue levels (MRLs) for the benzimidazole substances carbendazim and thiophanate‐methyl. Specifically, EFSA was asked to assess whether thiophanate‐methyl or carbendazim has clastogenic potential and, in case clastogenic potential can be excluded, to derive toxicological reference values necessary for consumer risk assessment and assessment of maximum residue levels (MRLs). Although these active substances are no longer authorised within the European Union, MRLs were established by the Codex Alimentarius Commission (codex maximum residue limits; CXLs), and import tolerances are in place. Based on the assessment of the available data, toxicological reference values and MRL proposals were derived and a consumer risk assessment was carried out. Some information required by the regulatory framework was found to be missing and a possible acute risk to consumers was identified. Hence, the consumer risk assessment was considered indicative only and all MRL proposals derived by EFSA still require further consideration by risk managers. In October 2022, to ensure that MRLs derived by EFSA in its assessment of 2021 are safe for consumers also in view of endocrine‐disrupting properties, EFSA was requested to carry out a follow‐up assessment taking into account the scientific criteria for identifying endocrine disruptors (ED). Based on the outcome of the assessment, the experts agreed that the reference values are also covering the concern related to the identified hazards indicative of endocrine disruption for thiophanate‐methyl. No further considerations on the impact of the ED assessment on the current reference values were needed for carbendazim since the ED criteria are not met for this substance. Therefore, the risk assessment and the MRL recommendations derived in 2021 are confirmed.
On 20 February 2024, EMEA, one of the founding organisations of the Brain Capital Alliance, organised an online expert meeting on “Challenges and... The post EMEA organises online expert meeting on the importance of exercise and physical movement, as keys in mental health and cognitive development of populations appeared first on EMEA.
Industry leaders spanning almost 20 industrial sectors presented ‘the Antwerp Declaration for a European Industrial Deal’ to Belgian Prime Minister, Alexander De Croo and Commission President, Ursula von der Leyen. The post Antwerp Declaration for a European Industrial Deal – Industry leaders call for 10 urgent actions to restore competitiveness and keep good jobs in Europe appeared first on Pro Carton.
Clinical Trials Information System Webinar: Last Year of Transition, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 25 March 2024, 13:00 (CET) to 25 March 2024, 17:30 (CET)
Cancer Medicines Forum workshop: April 2024, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 5 April 2024, 13:00 (CEST) to 5 April 2024, 18:00 (CEST)
Cancer Medicines Forum workshop, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 5 April 2024, 13:00 (CEST) to 5 April 2024, 18:00 (CEST)
CONEBI speaks at the 2024 Inland Transport Committee of the United Nations – Economic Commission for Europe (UNECE) – about Partnerships for Climate Action and jointly with WBIA commends UNECE efforts to develop a global definition of a Cycle on 20 February 2024 Switzerland, 20 February 2024 – Manuel Marsilio, General Manager of CONEBI was invited […]
Paediatric Committee (PDCO): 20-23 February 2024, Online, European Medicines Agency, Amsterdam, the Netherlands, from 20 February 2024 to 23 February 2024
Today 73 industry leaders spanning almost 20 industrial sectors presented ‘the Antwerp Declaration for a European Industrial Deal’ to Belgian Prime Minister, Alexander De Croo and Commission President, Ursula von der Leyen. The declaration underlines the commitment of industry to Europe and its transformation and outlines urgent industry needs to make Europe competitive, resilient, and […]
The periods within which peak concentrations could be exceeded are shown by light blue arrows, based on the trend of the past 10 years in total greenhouse gas concentrations and without allowing for a temperature overshoot (based on IPCC, 2019).
Network users training for Regulatory Procedure Management 1st roll-out on IRIS, Online, from 16 January 2024, 10:00 (CET) to 16 January 2024, 12:00 (CET)
The “rise of the machines” has played a critical role in advancing medical research and improving accuracy of diagnostic precision for decades, transforming the way we monitor new and existing disease...
Committee for Medicinal Products for Human Use (CHMP): 19-22 February 2024, European Medicines Agency, Amsterdam, the Netherlands, from 19 February 2024 to 22 February 2024
Sociedade Portuguesa de Inovação (SPI), a consortium member of INPACE project, attended the Kick-off Meeting that took place in Nice, France, from February 12th to 13th, 2024.
WARSAW, 16 February 2024 – The reported death of Alexei Navalny while serving a lengthy prison sentence is a tragedy that follows years of unjust imprisonment and the denial of his rights, including to a fair trial, the OSCE Office for Democratic Institutions and Human Rights (ODIHR) said today. “I am deeply saddened by the news of Alexei Navalny’s death,” said ODIHR Director Matteo Mecacci. “From the very beginning, Mr Navalny’s imprisonment was a fundamental violation of the right to voice dissent as well as the right to a fair trial.” ODIHR calls on the Russian authorities to launch an immediate and credible investigation into the circumstances in which he died, and to allow Mr Navalny’s representatives full access to it. ODIHR condemns the imprisonment of any opposition politician merely for expressing their political views, and calls for their release from detention. Justice systems must remain independent of politics and never be instrumentalized to silence dissenting voices. ODIHR calls on the Russian Federation to respect its obligation to ensure the health and welfare of all those in custody, and reminds the authorities that all OSCE states have committed to respect the rights of prisoners. They have also committed to guarantee the right to a fair trial and the independence of the judiciary. In particular, states have committed to guaranteeing a fair and public hearing by a competent, independent and impartial tribunal established by law.
Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the proposed modification of the terms of the authorisation regarding the maximum inclusion level of a feed additive consisting of nonanoic acid for all pigs and poultry species. Nonanoic acid is currently authorised for use as a sensory additive (functional group: flavouring compounds) for all animal species at a recommended maximum content of 5 mg/kg complete feed. The applicant is requesting a modification of the authorisation to increase the recommended maximum content of the active substance from 5 to 100 mg/kg complete feed for all poultry and pig species. In support of the safety of the additive at the new proposed level, the applicant provided tolerance trials in the target species. The FEEDAP Panel concludes that nonanoic acid is safe for all growing poultry species and Suidae at 100 mg/kg feed. The Panel cannot conclude on the safety of the new proposed level (100 mg/kg complete feed) for laying hens, turkeys for breeding, minor poultry species for laying/breeding and reproductive Suidae. However, FEEDAP Panel considered that nonanoic acid is safe at 10 mg/kg complete feed in laying hens, turkeys for breeding, minor poultry species for laying/breeding and 20 mg/kg complete feed for reproductive Suidae. The use of the feed additive in animal nutrition under the conditions of use proposed is of no concern for the consumer and the environment. Due to the lack of data, the FEEDAP Panel cannot conclude on the potential of the additive to be a skin and eye irritant neither a dermal nor respiratory sensitiser. No further demonstration of efficacy is necessary.
The European Investment Bank (EIB) announced a new €143 million loan to support the Hellenic Foundation for Research and Innovation’s (HFRI) research and development (R&D) activities in public higher education institutions and research centres across Greece.
The charts show: Top figures: the temporal development in the number of species of each biogeographical affinity group (Atlantic, Boreal, Lusitania and Unknown) by marine region (Greater North Sea, Baltic Sea, Celtic Seas and Bay of Biscay and the Iberian Coast). Bottom figures: the temporal development of the ratio between Lusitanian and Boreal species and sea surface temperature by marine region to investigate correlations.
Objective: The global burden of HIV remains a critical public health challenge, particularly in sub-Saharan Africa, home to over two-thirds of individuals living with HIV. HIV self-testing (HIVST) has emerged as a promising strategy endorsed by the World Health Organization to achieve UNAIDS targets. Despite its potential, challenges persist in linking self-testers to care post a positive result. Digital health interventions, including chatbots and mobile applications, offer innovative solutions to address this gap. However, a comprehensive bibliometric analysis of the collaboration and growth in the literature at the intersection of HIVST and digital interventions is lacking.Methods: The study employs a bibliometric approach, leveraging data from the Web of Science, to analyze the characteristics, citation pattern and content of 289 articles spanning 1992–2023. The analysis involves performance assessment, scientific collaboration analysis, science mapping, and content analysis. Key bibliometric indicators, such as annual growth rate, citation impact, and authorship patterns, are explored. Collaboration patterns among countries, institutions, and authors are elucidated, and thematic mapping provides insight into the key research themes.Results: The analysis reveals a dynamic and expanding field, with an annual scientific growth rate of 12.25%. Notable contributions come from diverse sources, including North America, Europe, and Africa. High-impact journals such as JMIR mHealth and uHealth play a crucial role in disseminating research findings. African authors, including Lebelonyane R, Ford N, and Lockman S, feature prominently, reflecting a positive trend in diverse authorship. Co-citation analysis highlights influential manuscripts, with systematic reviews dominating the top-cited articles. Collaboration analysis underscores strategic partnerships globally, particularly involving the United States, Australia, South Africa, and the United Kingdom.Conclusion: This bibliometrics analysis provides a comprehensive overview of the digital health landscape in HIVST and linkage to care. It identifies key contributors, high-impact journals, and collaborative networks. The thematic map reveals nuanced research domains, including alcohol dependence, men’s health, outcomes, and user acceptance. The findings offer insights for researchers, policymakers, and practitioners, guiding future directions in the evolving intersection of HIVST and digital health interventions.
Dans le cadre de ce webinaire, organisé par le projet SCORE financé par l’UE au titre d’Horizon 2020, des experts expliqueront comment déployer et exploiter des réseaux de capteurs à faible coût et présenteront certaines initiatives scientifiques citoyennes couronnées de succès dans le cadre du projet SCORE. Elles peuvent, entre autres, contribuer à donner aux communautés les moyens de comprendre et de relever les défis locaux du changement climatique.
Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety of a feed additive consisting of endo‐1,4‐β‐d‐mannanase produced by Thermothelomyces thermophilus DSM 33149, intended for use as a zootechnical additive (functional group: digestibility enhancers) for chickens for fattening, turkeys for fattening, minor poultry species for fattening and ornamental birds. The safety and efficacy of the additive have been already assessed previously; however, the FEEDAP Panel could not conclude on the safety of the additive for the target species, consumers and the users due to lack of reliable data on the potential genotoxicity of the additive. In the present assessment, the applicant submitted a new in vitro mammalian cell micronucleus test. After the assessment of the data newly submitted, the FEEDAP Panel concluded that the use of the feed additive in animal nutrition under the conditions of use proposed is of no concern for target species and consumer safety. The additive is not irritant to the eyes or skin. Owing to the proteinaceous nature of the active substance, the additive should be considered a respiratory sensitiser. The Panel cannot conclude on the potential of the additive to be a skin sensitiser.
Multi-stakeholder webinar on the HMA-EMA Catalogues of real-world data sources and studies, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 4 March 2024, 10:00 (CET) to 4 March 2024, 12:00 (CET)
Registradas el 14 de febrero de 2024, abordan el contexto ambiental, la salud como prioridad, el control de la calidad del aire, el contexto de movilidad y emisiones, los objetivos de la propuesta, el simpacto ambiental de la ZBE propuesta, y aportan 10 sugerencias concretas para mejorar el proyecto de Ordenanza de la ZBE La entrada Presentan alegaciones a la aprobación in la aprobación inicial de la Ordenanza Municipal por la que se regula una zona de bajas emisiones en el municipio de Valladolid aparece primero en Ecologistas en Acción.
Commission Implementing Decision (EU) 2024/564 of 14 February 2024 on harmonised standards for solid fuel boilers and packages of a solid fuel boiler, supplementary heaters, temperature controls and solar devices
The figure shows the percentage of monitoring sites with threshold exceedances of pesticides in surface waters, different sized rivers, lakes and groundwater in European countries. This was used to examine threshold exceedances according to Surface Waters; Rivers, small; Rivers, medium; Rivers, large; Lakes, and Groundwater.
The figures show the percentage of monitoring sites with exceedance of effect thresholds or quality standards, set by European or national regulatory standards, and weighted by country area to reduce the impact of uneven data reporting. For surface waters, EU environmental quality standards and (in the absence of those) national regulatory standards were used, reflecting the lowest ecotoxicologically-based effect threshold. Effect thresholds were identified for 116 out of 237 pesticides (49%). The exceedances included here refer to those 116 pesticides. For groundwater, the Groundwater Directive quality standard of 0.1µg/l was used to identify exceedance. Twelve non-relevant metabolites (nrM) were excluded from the assessment.
NOTICIA: El curso de especialización, coordinado por la Oficina de Proyectos Internacionales (OPI) de la Universidad Politécnica de Madrid, tiene una carga lectiva de 375 horas (15 ECTS) que se reparten en actividades docentes, de evaluación, trabajos prácticos y visitas presenciales que, este año, se van a realizar a la Representación de la Comisión Europea en Madrid, a la estación de
Polo Strategico Nazionale (PSN) continues to serve as the main facilitator of Italy’s digital transformation, thanks also to the support of the main Italian financial institutions and the European Investment Bank (EIB).
Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) meeting - April 2024, Online, European Medicines Agency, Amsterdam, the Netherlands, from 12 April 2024, 14:00 (CEST) to 12 April 2024, 16:00 (CEST)
Technical Webinar: Regulatory Procedure Management for PLM in IRIS for Network Users, Online, European Medicines Agency, Amsterdam, the Netherlands, from 27 February 2024, 14:00 (CET) to 27 February 2024, 16:00 (CET)
Statement by the High Representative on behalf of the European Union on the alignment of certain third countries with Council Decision (CFSP) 2024/385 of 19 January 2024 establishing restrictive measures against those who support, facilitate or enable violent actions by Hamas and the Palestinian Islamic Jihad.