This article contains information about Drugs and Cosmetics act 1940 (D&C act 1940) and Drugs and cosmetics rules 1945. Drugs and Cosmetics act 1940 (D&C act 1940) What is mean by Drugs and Cosmetics...
This article contains Comprehensive review on Tablet compression with Challenges and Solutions Tablet Compression Challenges and Solutions Tablet Compression Introduction : Tablet Compression is a manufacturing process used to convert...
This article contains Operation and Calibration of Friability test apparatus. Operation & Calibration of Friability test apparatus What is mean By Friability Test ? This test is used to test the durability/Friability of tablets...
This article explains the detailing on Equipment calibration and Instruments used for calibration of equipment which is used in pharmaceutical industry. EQUIPMENT CALIBRATION What is mean by Equipment Calibration: Calibration verifies the readings of a...
This article describes Types of Tooling used in the pharmaceutical industry to manufacture Tablet Formulations. Types of Tooling in Compression Machines: Description: Tablet compression machines are made by keeping view of type of Punches and...
What is Mean by Drug Master File I/II : Introduction/ Description: Drug Master File or DMF is a document prepared by a pharmaceutical manufacturer and submitted solely at its discretion to the appropriate regulatory authority...
This article contains the list of Global Drug Regulatory Authorities. What is mean by Drug Regulatory Authorities and what are there Roles: Drug Regulatory Authorities are a government authorities have responsibility for granting licenses,...
This article contains the Differentiation between Good manufacturing practices (GMP) and Current Good manufacturing Practices (cGMP). Differentiation of GMP Vs cGMP Introduction : GMP and cGMP are crucial regulations in the pharmaceutical industry to...
