Regulatory Aspects of Advanced Therapy Medicinal Products in the EU 2015
12 May 2015
Webinar
Key Topics
Committee for Advanced Therapies (CAT)
Introduction
Hospital exemption
Stem cells
Scientific recommendation on classification
Relevant guidelines
Certification procedure
Who should Attend
Project Managers
Senior management
Project Managers
Medical writers
QA / Compliance personnel
CRAs and CRCs
Clinical Research Scientists
Investigators
Consultants
QA / QC Auditors and Staff
Past Events
Regulatory Aspects of Advanced Therapy Medicinal Products in the EU 2015 - 12 May 2015, Webinar (51454)
Regulatory Aspects of Advanced Therapy Medicinal Products in the EU 2026
Important
Please, check "Regulatory Aspects of Advanced Therapy Medicinal Products in the EU" official website for possible changes, before making any traveling arrangements
Event Categories
Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Medical device, Medical laboratories, Pharma
