ECA Certified Pharmaceutical Development Manager

Not only in the manufacturing of marketed products (c)GMP-Compliance is mandatory. Also in the manufacturing of IMP supplies, compliance with the applicable GMP Guidelines is obligatory. But which GMP and GCP requirements are the applicable ones? And do the requirements differ from clinical phase 1 to phase 3? And how do I apply them?

This Certification Programme has been designed by the ECA to broaden your knowledge and to consolidate the various aspects which need to be considered in a successful development of a new pharmaceutical product.

Courses and Conferences acknowledged

To receive the certificate, the applicant must attend three out of the following courses/conferences. After attending the third course, the applicant obtains the certificate “ECA  Certified Pharmaceutical Development Manager”.

  • GMP meets Development
  • ICH Q8 Training Course
  • How to write the Quality Part of an IMPD
  • Pharmaceutical Packaging Systems – Part 1 Development
  • Granulation & Tableting
  • GMP meets GCP
List of all courses and conferences currently offered and acknowledged in this programme

Your Questions

For questions relative to the ECA Certified Pharmaceutical Development Manager, please contact enquiry@gmp-compliance.org.

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