Regulatory Aspects of Advanced Therapy Medicinal Products in the EU 2015 is a webinar that covers topics such as:
- Committee for Advanced Therapies (CAT)
- Introduction
- Hospital exemption
- Stem cells
- Scientific recommendation on classification
- Relevant guidelines
- Certification procedure
Regulatory Aspects of Advanced Therapy Medicinal Products in the EU 2015 is intended for:
- Project Managers
- Senior management
- Project Managers
- Medical writers
- QA / Compliance personnel
- CRAs and CRCs
- Clinical Research Scientists
- Investigators
- Consultants
- QA / QC Auditors and Staff