GMP - PharmaRead

March 25, 2023

Tips and Techniques for Conducting Internal Audits of Pharmaceutical Facilities in Low- and Middle-income Countries

Pharmaceutical facilities are subject to strict regulations and requirements, as they deal with the production and distribution of medicine. To ensure that they are meeting these standards, it is essential to conduct regular internal audits. These audits are meant to evaluate and assess the facility’s compliance with regulations, identify areas of improvement, and implement corrective […]

March 20, 2023

The Essential Guide to GMP for Pharmaceutical Professionals: An Introduction to Its 20 Key Principles

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GMP is a set of guidelines that helps ensure that pharmaceutical products are consistently produced and controlled according to quality standards. In this blog post, we’ll be diving into the essential guide to GMP for pharmaceutical professionals, covering its 20 key principles. From manufacturing to quality control, we’ll explore each principle in an easy-to-understand manner. […]

August 27, 2022

10 steps to writing an effective cGMP guide for line staff in the pharmaceutical industry

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Pharmaceutical manufacturing is a highly regulated industry in which cGMPs (current Good Manufacturing Practices) must be followed in order to ensure the safety and efficacy of drugs. Writing an effective cGMP guide can be a daunting task, but there are a few key points to keep in mind that will help you create a document […]