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QUALITY & COMPLIANCERegulation of Pharmaceutical Products in Singapore By Maya M. Lakes, PhD, RAC The city/country of Singapore, a member of the Association of Southeast Asian Nations (ASEAN), has

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What is regulation of pharmaceutical products?

Regulation of pharmaceutical products refers to the set of rules and guidelines that govern the manufacturing, distribution, and marketing of pharmaceutical drugs to ensure their safety, quality, and effectiveness.

Who is required to file regulation of pharmaceutical products?

Pharmaceutical companies are required to file regulation of pharmaceutical products for each drug they intend to bring to market.

How to fill out regulation of pharmaceutical products?

Regulation of pharmaceutical products is typically filled out by submitting an application to the relevant regulatory authority along with all necessary documentation and testing data.

What is the purpose of regulation of pharmaceutical products?

The purpose of regulation of pharmaceutical products is to protect public health by ensuring that drugs on the market are safe, effective, and of high quality.

What information must be reported on regulation of pharmaceutical products?

Information such as composition, manufacturing process, preclinical and clinical data, labeling, packaging, and pharmacovigilance measures must be reported on regulation of pharmaceutical products.

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