Executive course on Drug Development and Regulatory Affairs
The program intends to solidify knowledge and skills of experienced employees working in the Pharmaceutical industry (pharmaceutical companies, biotechnology companies, regulators, CROs, academia, etc.). The program identifies the importance of retaining experienced employees by providing them with current tools and policies to work under high standards with minimum supervision. The program offers an opportunity to obtain a Diploma certificate on both International and National drug regulatory affairs. The program content is designed to define the framework for developing and testing a drug or a medical device and for understanding the regulatory aspects in India and abroad (mainly focused on Europe and USA).

The “Executive course on Drug Development and Regulatory Affairs” is offered by Centre for Regulatory Science, Prasanna School of Public Health (PSPH), Manipal Academy of Higher Education (MAHE) in collaboration with the European Center of Pharmaceutical Medicine (ECPM), University of Basel, Switzerland. The program intends to support organizations / individuals to invest in improving their knowledge and skills, under international standards with the best faculty members from Europe, USA and India who are from academia and from industry, following the world-class model from ECPM at University of Basel.
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