How the 2011 comitology reform changes for regulatory affairs professionals- Competencies of the European Commission and procedure changes- Essential information for food, pharma, health, tobacco, environment industries
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.
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.
Acquisire le competenze specifiche per l'individuazione delle opportunità di finanziamento europeo collegate alla cooperazione nel bacino del Mediterraneo e sviluppare le tecniche di redazione dei progetti necessari per l
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.
Why do US companies fight their battles in Europe? Is EU competition policy becoming antitrust politics? Broadcast live from Brussels and Washington D.C. - Presented in cooperation with the American Antitrust Institute (AAI)