10. - 12.10.2012

Heidelberg: GMP Compliance for Biopharmaceuticals and ATMP

During this three days seminar, the attendees will learn important GMP- and regulatory aspects of the development of biopharmaceuticals and ATMPs.

Dr. H. Horn will give several presentations covering GMP and regulatory aspects of biopharmaceuticals as well as process changes from development to commercial manufacturing. On the last day, specifically assigned to ATMPs, she will guide you on how to comply with GMP and regulatory requirements for ATMPs. You will learn how to prepare your dossier for Authorities and how to prepare for inspections. You will get detailed insight on the specifics for the development of ATMPs.


For more information please visit the following website:
http://www.gmp-navigator.com/daten/training/ECA_GMPComl_Biopharmaceuticals.pdf

 
(Conference organized by Concept Heidelberg)



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