Introduction EU GMP for Cannabis Industry

• 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

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.