Information détaillée concernant le cours
Quality in Pharmaceuticals -- FULL --
06.05.2021, 08:30-12:00 and 13:30-16:30, and 07.05.2021, 09:00-12:30
|Lang||Workshop language is English|
Ms Ann Stroemberg, Director Global Development Compliance, Global QA at Ferring Pharmaceuticals A/S, Copenhague, Danemark
Dr François-Xavier Abellan, Associate Director GQA Quality System at Ferring Pharmaceuticals, Saint-Prex, Switzerland
Mr Julien Boccadoro, CMC Project Leader at Ferring Pharmaceuticals, Saint-Prex, Switzerland
Pharmaceuticals are considered as the most highly regulated industries worldwide.
Quality, from research and development stages through production, testing and post-marketing surveillance by applying the principles of Quality by Design (QbD), Quality Assurance (QA), and the Good Practices (GxPs), is essential to ensure the safety, quality and efficacy of medicines.
The Quality in Pharmaceuticals course is designed for people who have no knowledge of the GxP in the pharmaceutical industry.
The Objective with this course is to understand the importance of Quality in the development and manufacturing of products in the pharmaceutical industry:
· You get to know the most important pharmaceutical regulations and their application areas
· You get a basic overview and understanding of the quality requirements applied in the pharmaceutical industry
· You get an overview of Pharmaceutical Development and Quality by Design principles
You become familiar with specific terms in the field of GxP and their meaning
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