[Call for Entries] Belgium Zodiac Design & Creative Contest
Entry your design for the 2023 BELGIUM ZODIAC DESIGN & CREATIVE CONTEST to be showcased during the 2023 New Year celebrations! Open until 9 October 2022 to all talents of Belgium and other European countries!
Empowering Teachers to realise the full potential of students with Dyslexia in an Education setting
This self-paced online course is designed to provide teachers in mainstream educational settings the knowledge and skills required to support the educational and social needs of students with Dyslexia in order to achieve their full potential.
Empowering Teachers to realise the full potential of students with Sensory Sensitivities
This self-paced online course is designed to provide teachers in mainstream educational settings the knowledge and skills required to support the educational and social needs of students with Sensory processing Difficulties.
Empowering Parents to realise the full potential of children and young people with Sensory Sensitivities
This self-paced online course is designed to provide Parents with useful and understandable information about sensory processing difficulties and to use strategies to maximise the child/young person’s full potential.
Empowering Parents to realise the full potential of children and young people with Dyslexia
This self-paced online course is designed to develop Parents’ knowledge and expertise in working positively with children and young people with Dyslexia in order to reach their full potential.
Webinar On Obtaining and Maintaining EU Compliance
This CE marking training will discuss the recent changes to MDD (Medical Device Directive), how to identify non compliance areas, contents of the technical file and essential requirements document.
In this Foreign Corrupt Practices Act (FCPA) webinar training understand the prohibited and exempted actions as per FCAP act, how to find the non compliance issues and how to implement FCPA compliance policies.
Attend this webinar to understand the process of a letter of credit and how to comply with letter of credit requirements to help reduce or prevent costly discrepancies.
In this Audit training learn how to make audit checklist an effective tool, by improving it through restructuring to drop the canned clause-based questions and identify the expected evidence.
When you get your 510(k) how to market your 510(k) , what communication strategy to adopt, what to do when FDA disagrees with your promotional positioning.
This highly interactive course will include detailed discussions of current regulatory expectations and is therefore suitable for individuals new to the pharmaceutical industry and also serves as a refresher course for others.
Learn how to differentiate and draw boundaries for GMP and GLP practices if done in same laboratory and how to transition a procedure in development to one used routinely.
In this HACCP webinar learn the required elements of conducting and documenting CCPs and process parameters and the five sources of HACCP validation as per FSIS guidelines.
This Food Safety training will teach you about how to use problem solving method steps and tools to eliminate the reoccurrence of process & product non-conformities .
Understand 10 step Risk based approach to validation, explore methods to decrease resource requirements and make documentation more manageable and understandable.
In this CSV seminar learn how to reduce validation project time, efficient documentation strategies, enhance system productivity and increase compliance with the New 21 CFR Part 11 regulations.
This webinar delves into what to (and not to) do when you receive communications from the IRS and also what to do when doing business with other federal, state and local regulatory agencies and lawmaking bodies.
Auditing and Administrating Human Resource Policie
This HR compliance virtual event will discuss about HR risk assessment, Recordkeeping, Retention and Destruction, Selecting and Administering Employment Policies, Legal Interviewing and Hiring Practices.
Learn steps to create a fool proof retention process and strategies for effective employee involvement and the low cost ways to motivate and energize employees.
This webinar will describe the distinctions that must always exist between contractors and employees based on standards used by the federal Department of Labor.
Learn in details how to accurately and completely process garnishment orders through the payroll department in compliance with federal and state requirements and regulations.
These are just a few of the nightmares that keep HR professionals awake at night. If these are the kinds of employee problems that are haunting you, we promise this webinar will help you get a better night
This health care reforms webinar will discuss the various categories of employer under health Care reform, impact of the reform and the steps to be ready for upcoming implementation dates.
This webinar provides an update of federal and state UI issues, assesses the risks and costs associated with UI taxes and benefits, and discusses effective UI tax management and cost control techniques.
This Pregnancy Discrimination claims related training will provide essential strategies for ensuring that those rights are observed while at the same time allowing for the smooth operation of your organization.
A detailed understanding of process validation for medical devices approach employing IQ, OQ, and PQ. Information to include in the protocols and reports, Statistical Process Control, Design of Experiments, usage of attribute.
This Medical device complaints handling webinar will discuss the best practices of complaint handling and how to include it in your CAPA program and how to apply risk management to the complaint handling system.
This Ethylene Oxide Sterilization Residuals regulation based webinar will provide a practical approach to fulfill requirements of the new ISO EO residual limits revised regulation.
This Medical device inspection webinar training will teach you A to Z of inspection starting with how to prepare to what to do during inspection, close-out interview, FDA
This presentation will review the QSR requirements for document change control, and provide a streamlined process - Many companies can spend MUCH LESS preparing MANY FEWER documents, and still be in compliance with the regulations;
This Integrated Risk Management Approach training in ISO 14971 will discuss how to incorporate risk management as per ISO 14971 in all phases of medical device development.
Learn how to successfully pass a clinical trial audit, how to prepare for it, where and how to identify the non compliance. Know FDA inspection strategy to identify areas of common deficiency.
This course reviews the investigator TMF required and additional content for a clinical trial - the activities of set-up, maintenance, and quality control and assurance will be discussed, as well as common deficiencies and challenges.
This clinical research ethics training will impart an understanding to regulatory compliance and clinical study personnel on the importance of ethics in clinical research .
This environmental monitoring training will review the best practices for setting environmental monitoring alert and action levels for viable and non-viable data including product bioburden.
Learn the scientific standards of drug development process, the regulations to follow in Phase I and how to manage each phase of drug development process.
This IFRS (International Financial Reporting Standards) webinar will discuss how to assign a fair value to financial instruments and how to comply with the changing rule for accounting for investment on financial statements.
This contamination control webinar will discuss how personnel practices, transferring items into cleanrooms, facility design, construction, and sporicidal chemistries are critical .
It is critical that a robust transfer program be put into place in order to head off issues. Unearthing issues at the drug development stage, rather than during routine manufacture, will improve the overall success of the project.
This Design validation 4 hour session will discuss how to write validation protocol and determine acceptance criteria. It will also explain the systematic approach to validate analytical procedures.
This interactive one-day course provides a thorough understanding of what makes water systems have microbial problems with proven solutions for microbial control, arguments for the micro lab.
The session will review the guideline to cover the key areas of compliance including: The role of the "Qualified Person", Packaging, labeling, reconciliations that should take place for each product and each production stage.
This DMFs (Drug Master Files) training will discuss the current review and enforcement climate within FDA and the manner in which drug master files (DMFs) are reviewed by FDA personnel.
Do you want to acquire more knowledge about EU funding opportunities and projects drafting and managing? do you want to become Policy Advisor and Project Consultant? come and ask for more information about the International Master in European Studies