Classroom 1 Day
47740931
In this training, you will interpret the requirements of the good manufacturing practice (GMP)
Description
In this training, you will interpret the requirements of the good manufacturing practice (GMP) Pharmaceuticals EU Directive for medicinal products for human and veterinary use, and for Medicinal Products and Active Substances used as Starting Materials with its application in the context of EudraLex Volume 4.
Objectives
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Audience
Pharmaceutical and medicinal products manufacturers, safety and quality managers, supervisors, internal auditors, consultants, and anyone interested in understanding and meeting the requirements of the GMP Pharmaceuticals EU Directive for medicinal products for human and veterinary use. |
Classroom 1 Day
47740931