In 2018, the Food and Drug Supervisory Agency (Badan POM) published Guidelines for Good Medicine Manufacturing Practices (CPOB) as a reference for the pharmaceutical industry and facilities that make medicines and/or medicinal substances to ensure that medicines and/or medicinal substances are made. consistently, meets the specified requirements and is in accordance with its intended use. The POM Agency has collected questions related to the points in the 2018 CPOB Guidelines from the pharmaceutical industry in Indonesia and held discussions with the National CPOB Team to prepare explanations for these questions. Questions & Answers (Q&A) Implementation of the 2018 CPOB Guidelines is an explanation of the requirements set out in the 2018 CPOB Guidelines.
Q & A The implementation of the 2018 CPOB Guidelines is expected to make it easier for the pharmaceutical industry to implement CPOB requirements, thereby increasing the independence of the pharmaceutical industry and increasing competitiveness in maintaining the quality of the products made.
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