Regulation of Advanced Therapy Medicinal Products in Europe 2013 is a webinar that covers topics such as:
Which technologies are covered
CAT and ATMP Structures
Non-clinical studies
Classification procedures
Certification of development work
Clinical Studies
Hospital Exemptions
Incentives
An overview of CMC requirements
Regulation of Advanced Therapy Medicinal Products in Europe 2013 brings together:
Quality
Regulatory Affairs
Manufacturing
Clinical
Import / Export
Supply Chain
General Management
Global Business Development
Documentation
Administrative Staff
Past Events
Regulation of Advanced Therapy Medicinal Products in Europe 2013 - 22 Jan 2013, Webinar (35406)
Important
Please, check "Regulation of Advanced Therapy Medicinal Products in Europe" official website for possible changes, before making any traveling arrangements
We use cookies to enhance your browsing experience, serve personalized ads or content, and analyze our traffic. By clicking "Accept", you consent to our use of cookies. You can manage your preferences or learn more by clicking "Customize" or visiting our Cookies Policy page.