European GMPs and the Role of the QP 27-28 June 2012 Bethesda, MD 20814 Please click here to view the program of this conference or course To book for this program, just click on the option: Book this option: Non-ECA Members (USD 1690,--) Book this option: ECA Members (USD 1590,--) Book this option: Government/Health Authorities (USD 750,--)
Dear Colleagues, The Pharmaceutical Industry is becoming more global due to international collaborations, mergers and acquisitions and more complex supply chains requiring companies to have a greater understanding of pharmaceutical legislation throughout the world. This is becoming increasingly evident by the number of non EU professionals contacting the European Compliance Academy and the Qualified Persons Association asking for more and more detailed information about the European GMPs and the unique role and responsibility of the EU QP. The European Compliance Academy ECA and the European QP Association, recognising this need for further professional knowledge development, intend to support the pharmaceutical industry outside Europe in understanding the European approach and legal framework in this respect. Therefore the QP Association has set up the programme at hand on European GMP requirements and the role of the QP. Representatives from the authorities as well as QPs and well-known experts will talk about the current issues and share their point of view. During the two post-conference workshops and, various case studies will be presented and discussed to come up with possible solutions. Make use of this event by exchanging experiences with your colleagues and by establishing informal contact and networking. I would like to invite you to this unique opportunity, and I look forward to meeting you. Best regards, Dr Bernd Renger Chairman of the Qualified Person Association