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Category: Regulatory Affairs

Regulatory Affairs

Pharmaceutical MA Extension (Visa No. / Reg. No.) in Vietnam

Pharmaceutical Marketing Authorization / Visa Number / Registration Number Extension in Vietnam The Marketing Authorization (MA) is the official license issued by a competent authority that allows a pharmaceutical product …

Regulatory Affairs

CPP Requirements for Imported Drug Registration in Vietnam

CPP Requirements for Imported Drug Registration in Vietnam The Certificate of Pharmaceutical Product (CPP) is one of the most important documents required when registering imported drugs in Vietnam.  In Vietnam, …

Regulatory Affairs

GMP Assessment for Foreign Pharmaceutical Manufacturers

GMP assessment for foreign pharmaceutical manufacturers when registering drugs in Vietnam GMP assessment for foreign pharmaceutical manufacturers is a mandatory step when registering imported drugs in Vietnam to ensure product …

Regulatory Affairs

Imported Drug Registration in Vietnam

Imported Drug Registration in Vietnam under Circular 08/2022/TT-BYT Imported drug registration in Vietnam is governed by Circular 08/2022/TT-BYT and related laws. This article offers a step-by-step overview of how to …

Recent Posts

  • Pharmaceutical MA Extension (Visa No. / Reg. No.) in Vietnam
  • CPP Requirements for Imported Drug Registration in Vietnam
  • GMP Assessment for Foreign Pharmaceutical Manufacturers
  • Imported Drug Registration in Vietnam

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