E-DRUG: 5-day International Certificate Course-Pharmaceutical Product Quality & Regulatory Affairs
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Dear Members,
Greetings from Empower.
We are pleased to announce that Empower, CILT accredited Center of
Excellence for Global Health Supply Chain Management, is organizing a *5-day
classroom training on Pharmaceutical Product Quality and Regulatory Affairs*,
in collaboration with Indian Pharmacopeia Commission, The Ministry of
Health and Family Welfare, Govt. of India.
The training is scheduled from *17th-21st April, 2017* in *New Delhi, India*
The objective of the course is to promote Access to Medicines by
addressing pharmaceutical regulatory barriers, through collaborative
training methodologies and cohesive discussion between regulators and
manufacturers. The course also aims to provide information on various
pharmaceutical reference standards and their impact on global access to
medicines.
The key topics being covered are:
- Regulatory Harmonization: Global Perspectives
- GMP inspection (in theory)- Product and Process Flow in GMP
- GMP inspection (in practice)- Visit to a pharmaceutical manufacturer
- Good Laboratory Practices: Concepts, Standards, Accreditations
- Analytical testing, Reference Standards (International, Indian
Pharmacopeia)
- Analytical testing (in practice), Analytical Method Verification
- Laboratory visit: Hands on session on testing
Currently, we are offering an early bird and group registrations discount.
Interested participants can fill in the online application in the link here
http://empowerschoolofhealth.org/classroom-courses/internationa
l-certificate-course-on-pharmaceutical-product-quality-and-regulatory-
affairs-545
Please feel free to email us at training@empowerschoolofhealth.org.
Regards
Ms. Kavya RS
Training & Education Coordinator
Empower School of Health | New Delhi . New York
(India) | info@empowerschoolofhealth.org
Kavya RS <info@empowerschoolofhealth.org>