Integración de procesos de buenas prácticas de manufactura en una industria farmacéutica de medicamentos inyectables

Abstract

Good manufacturing practices are one of the sanitary regulations necessary to obtain a certification of pharmaceutical quality. For decades, GMPs have been implemented and improved through strategies to produce safe and effective medicines that provide well-being to the client. Pharmaceutical industries that are engaged in the manufacture of injectable drugs must strictly comply with all the requirements because by being administered parenterally and having contact with the bloodstream, they can affect the safety of the patient and the credibility of the product. This work through the use of the bibliographic review proposes integration strategies of good manufacturing practices for a pharmaceutical company of injectable drugs, in order to improve the quality of its drugs. Quality control in the pharmaceutical industries of injectable drugs is important to indicate if the drug meets the requirements and implement strategies that incorporate good manufacturing practices to ensure the efficacy, quality, and safety of their drugs. A bibliographical research was carried out presenting seven practical cases of different injectable pharmaceutical industries that seek to strengthen their weaknesses. On the other hand, strategies for the integration of good manufacturing practices processes were proposed, with the points that are presented in order to reduce the risks inherent in any pharmaceutical production. Finally, the strategies that have been presented in the different cases determine that, if there is an integration of the BPM techniques of the drugs in the pharmaceutical industries of injectables analyzed.