Introduction EU GMP for Cannabis Industry

In this training, you will interpret the requirements of the good manufacturing practice (GMP)

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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

  • Understand the principles, guidelines, and application of GMP for medicinal products as laid out in Directive 2003/94/EC for medicinal products for human use and Directive 91/412/EEC for veterinary use
    Understand the benefits of implementing GMP principles 
    Interpret requirements within EudraLex Volume 4 in the context of an audit, and from an auditor's perspective
    Practice interpreting the standard to identify non-conformances




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.



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    47740931

    1 Day

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