Target audience: The course is designed for professionals working in pharmaceutical manufacturing industry, medicine regulation, GMP-relevant areas and GMP inspectorates.
Date: September 19 – October 31, 2016 |Course duration: Six (6) weeks | Time investment per week: 4 hours per week
Cost: 450 euros per participant. A discount of 60 euros applies to all participants from low and middle-income countries (LMIC)
Development of medicines regulations
Overview of good manufacturing practice (GMP)
Good practices in production and quality control
Qualification and validation
Dr Christina Foerg-Wimmer is an international pharmaceutical consultant with experience in private, public and international organizations as well as NGOs, mainly in developing and emerging countries. She has presented papers at several international congresses and published several pharmaceutical articles in renowned international journals.
Pharmacist by profession with Ph.D. from the Swiss Federal Institute of Technology (ETH), Zurich
Regional and country experience: Germany, Ghana, China, USA, Switzerland, South Africa, Ethiopia, Vietnam, Thailand, USA including East Africa, Asia Pacific regions.
Area of expertise: Pharmaceutical production, medicine regulation, clinical trials, pharmaceutical technology, feasibility studies, project evaluations, capacity development, proposal development, health systems development, research and development.
phone: +31 348748701
address: Polanerbaan 11, 3447 GN, Woerden, The Netherlands