by Dr. Yashashwini Reddy | 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 Dr. Yashashwini Reddy | 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...
by Dr. Yashashwini Reddy | Jul 18, 2024
What is BCS classification? According to the BCS classification system, drugs are classified based on their solubility and intestinal permeability. The full form of BCS is the Biopharmaceutics Classification System. Drugs are classified by considering their...
by Dr. Yashashwini Reddy | Jun 3, 2024
What is an Investigational New Drug (IND) Application and When is it Required?” In this article you are going to learn about IND and its types and when an IND is required. Generally, in the US to conduct clinical trials i.e. for the administration of...
