Jean-Marc Libersa

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GMP Support
Consultant
Jean-Marc Libersa has worked for 37 years in the pharmaceutical industry (human and veterinarian) and is currently a consultant for GMP support. Previously, he served as Quality Director for a CMO, with overall responsibility for 15 plants manufacturing drug products and drug substances.

Related Articles

Serialization model
Features
Ten Frequently Asked Questions about Serialization

To meet the EU serialization deadline on 9 February 2019, pharmaceutical companies and their contractors have had to reorganize their manufacturing lines and logistics to ensure compliance with the EU’s Falsified Medicines Directive (FMD) of 2011 and the EU Commission Delegated Regulation 2016/161 of 2016. Worldwide, other anticounterfeiting regulations are already in place or coming soon in...