The Management of Clinical Trials – GMP meets GCP

In the development of new pharmaceutical products, it is a challenge to design and initiate sound and appropriate studies. In this course on 15/16 November in Berlin, Germany, representatives from authorities as well as specialists from the pharmaceutical industry and service providers will therefore share their expert knowledge about important aspects of IMP Supplies and the Management of Clinical Trials. The course will cover all essential aspects relative to the organisation and management of the supplies, their distribution and things to consider during the study. It will also address how the various regulations lead the way, and it will elaborate the important interfaces between GMP and GCP. Find more information at http://www.gmp-compliance.org/eca_seminar_1443.html.

Contact:
On behalf of the European Compliance Academy (ECA)
Wolfgang Heimes
P.O. Box 10 21 68
69011 Heidelberg, Germany
E-Mail: heimes@gmp-compliance.org

About the ECA
Founded as an independent organisation in 1999, the European Compliance Academy’s (ECA) goal is to facilitate the move towards a harmonised set of GMP and regulatory guidelines. It supports the Pharmaceutical Industry and Regulators through providing information on and interpretation of new or updated guidances. For that purpose the ECA developed a range of tools like the GMP Guideline Manager CD-ROM, and also organises international education courses, webinars and conferences around GMP, regulatory compliance and currently discussed subjects. For further information on the ECA please refer to www.gmp-compliance.org.

This release was published on openPR.