A multinational manufacturer of cardiovascular devices recently engaged SeerPharma to conduct a comprehensive mock US FDA audit of their operations in Singapore. The audit was conducted against US FDA 21 CFR Part 820 – Quality System Regulation (21 CFR 820). SeerPharma reviewed relevant documentation remotely and then spent three days on-site...
SeerPharma have partnered with Temasek Polytechnic’s Centre of Innovation for Complementary Health Products (COI-CHP), to assist companies involved with Pharmaceuticals, Biologicals, Complementary Medicines, Traditional Chinese Medicine and Cosmetics, help ensure their Facilities and Operations are GMP compliant; their products are manufactured...
The Parenteral Drug Association (PDA) is a leading global provider of science, technology and regulatory information and education for the pharmaceutical and biopharmaceutical community. Founded in 1946 as a nonprofit organization, PDA is committed to developing scientifically sound, practical technical information and resources to advance science...
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