North America's leading Solar event dedicated to Asset Management and O&M.

Now available to watch on-demand! #USOW20 Virtual Conference - Your Gateway into the U.S. Offshore Wind Industry

The international meeting point of the Hydrogen and Fuel Cell community in the USA

The international meeting point of the Hydrogen and Fuel Cell community in the USA

Photonics West, the #1 laser, photonics, biomedical optics conference

BiOS is the world's largest and most prestigious international biomedical optics and imaging conference, encompassing clinical, translational, and fundamental R&D.

SPIE Photonics West Exhibition is the premier photonics and laser event.

BiOS Expo is the world's largest biomedical optics and biophotonics exhibition.

Photonics West, the #1 laser, photonics, biomedical optics conference: 20,000 attendees, six renowned symposia, and 4,800 R&D presentations covering a wide range of papers on biomedical optics, biophotonics, translational research, and more.

BiOS is the world's largest and most prestigious international biomedical optics and imaging conference, encompassing clinical, translational, and fundamental R&D.

Optics and Photonics for Sensing and Security

IRSET 2014

SPIE Photonics West Exhibition is the premier photonics and laser event.

SPIE Photonics West is the largest and most influential conference for biophotonics, biomedical optics, industrial lasers, optoelectronics, microfabrication, optical MEMs, and green photonics.

Building Innovation in Multiplatform TV Content Development

SPIE Photonics West is North America's largest optics and photonics exhibition.

Photonics West includes the entire spectrum of light-driven technologies and attracts researchers and product developers from around the world.

Defense, Security, and Sensing has moved to Baltimore

SPIE Photonics West is North America's largest optics and photonics exhibition.

Photonics West includes the entire spectrum of light-driven technologies and attracts researchers and product developers from around the world.

BiOS is the world's largest and most prestigious international biomedical optics and imaging conference, encompassing clinical, translational, and fundamental R&D.

SPIE LASE presents the latest fundamental and applied research on new laser sources and applications.

OPTO 2012 addresses the latest developments and advances in a broad range of optoelectronic technologies and their integration for a variety of applications.

Share your research and development activities with colleagues, sponsors, customers, technologists, engineers, scientists, and clients in the growing industry of Micro- and Nanofabrication of MEMS and MOEMS.

Understand 10 step Risk based approach to validation, explore methods to decrease resource requirements and make documentation more manageable and understandable.

This is an introductory course for section by section understanding of ISO 13485 requirements of a quality management system.

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.

How to Use excel spreadsheet for GXP data and reduce validation cost and time.

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.

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.

This workplace hostility prevention program will provide best practices for mitigating organizational hostility and violence.

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 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.

This China life science compliance based webinar will discuss the regulatory structure and requirements for compliance with Chinese SFDA regulations.

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.

Understanding of latest FDA guidance requirements and expectations related to medical device tracking and what are the new changes.

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.

Attend this webinar to understand how to manage risk in hiring, how to do background checks/screening, employee assessment.

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.

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 contamination control webinar will discuss how personnel practices, transferring items into cleanrooms, facility design, construction, and sporicidal chemistries are critical .

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 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.

Learn in details how to accurately and completely process garnishment orders through the payroll department in compliance with federal and state requirements and regulations.

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.

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 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.

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 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 webinar will describe the distinctions that must always exist between contractors and employees based on standards used by the federal Department of Labor.

What are you doing to illustrate the cost-benefit relationship your safety program has on your company

This 510(k) webinar will help you understand the proposed changes to 510(k) process in 2011 and the regulatory process of implementing it.

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.

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 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 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 training will include hypothetical fact scenarios that present common recordkeeping issues encountered by facility record keepers.

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

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 CLIA Laboratory Inspection training will discuss the salient features of laboratory inspection as per CLIA inspection guidelines.

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.

Understanding of IRB application components and how to find out and fix problem areas before it threaten your trial to fail.

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.

The key is complete and proper training from experts who has worked on hunderds of 510(k)s, de novo submissions, PMAs and combination products.

This webinar explains these requirements from QSR and explains the role of each document type. The webinar uses the QSR preamble to explore FDA

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.

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;

Learn how to differentiate employees and independent contractors as per IRS rule and understand the correct process to compensate them.

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 FDA cGMP training webinar will discuss US FDA

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 how to select the wellness program most effective for your team with respect to ethics and also benefits of increasing the engagement.

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.

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.

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 .

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.

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 the scientific standards of drug development process, the regulations to follow in Phase I and how to manage each phase of drug development process.

Attend this webinar to understand the background as well as practical strategies for responding to workplace crises.

Workplace harassment can be destructive. Learn the in