Regulation of Advanced Therapy Medicinal Products in Europe 2013
22 Jan 2013
Webinar
Description
Topics
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
Who should Attend
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
