Date(s) - 16/01/2018 - 17/01/2018
The Qualified Person (QP) is assuming the responsibility of GMP and GDP compliance of the entire
processes that participate in the medicines supply chain: primary manufacturing (raw materials),
transport, warehousing, distribution, secondary manufacturing (medicines), packaging and
distribution to hospitals and pharmacies.
The objective of this event is to offer an opportunity to share the current requirements and practical
interpretations, having open discussions on the different approaches than can be followed to meet
the expectations of the authorities in a reasonable and efficient manner. The main conclusions of this
meeting will constitute a valuable foundation for AFA to prepare the 2018 GDP Audit Plan for AFA
customers in Central Europe.
Professionals from the API and medicines industry having responsibilities in:
The meeting will be performed using German & English language.
Download the updated event briefing by clicking here.