Full Day Pre-Conference Session: Specific Requirements for IMPs

Full Day Pre-Conference Session: Specific Requirements for IMPs

Madrid, Spain

Course No 15361


Costs

This conference already took place.

If you have any questions, please contact us:
Tel.: +49 (0)6221 / 84 44 0 E-Mail: info@gmp-compliance.org

Objectives



Programme

Full Day Pre-Conference Session on 30 November 2016

Specific Requirements for IMPs
Facilitated by:
IMP Working Group

New legislation impacting IMP QPs
Revised Annex 16 – lessons learned
Advanced Therapy Medicinal Products (ATMPs): regulatory requirements, GMP and the grey zones
Quality Assurance Agreement / QP to QP agreement for clinical trial manufacture
Interactive sessions
Q & A sessions

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