by Naveen kumar | Oct 24, 2024
Good Laboratory Practices (GLP) in the pharmaceutical industry are a set of internationally recognized standards that ensure the quality, consistency, and integrity of non-clinical studies. These practices are critical for ensuring that the data generated during drug...
by Naveen kumar | Oct 22, 2024
Quality by Design (QbD) in Pharmaceuticals: Enhancing Drug Development and Manufacturing In the pharmaceutical industry, ensuring product quality is crucial to patient safety and regulatory compliance. Quality by Design (QbD) is a systematic approach to drug...
by Naveen kumar | Oct 22, 2024
Good Automated Manufacturing Practices (GAMP): Ensuring Quality in Pharma Automation In today’s fast-paced pharmaceutical industry, automation has become a key driver for improving efficiency, consistency, and maintaining the highest quality standards. To ensure...
by Naveen kumar | Oct 21, 2024
The specifications of the disintegration test apparatus are crucial to ensure accurate and consistent results when evaluating the quality of immediate-release tablets. Each component and the movement of the apparatus are precisely designed to simulate conditions...
by Naveen kumar | Oct 18, 2024
Process Research and Development (R&D) in Pharmaceuticals The Process Research and Development (Process R&D) department in the pharmaceutical industry is responsible for developing, refining, and optimizing the methods used to manufacture drugs. This critical...
