A stability chamber works on the principle of maintaining the relative humidity (RH) and temperature of the chamber with the help of thermostats and water reserved in the chamber. As per the law of physics, the air can maintain higher humidity with the help of high temperatures in the chamber because the high temperatures […]
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Principle of autoclave The autoclave functions to sterilize the subjected material by generating steam pressure inside the chamber at a standard vaporizing temperature, maintaining the conditions for a certain time frame. The whole process is moist heat sterilization which is the principle of autoclave. What is an autoclave? An autoclave is a machine designed in
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USFDA approval is a big milestone for any pharmaceutical manufacturing facility. If you are looking to export medicines to the US then you must have your facility approved by the USFDA. A pharma company can only sell direct products in the US market if they have got approval from the USFDA department. Every drug manufacturer
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 FDA guidelines for high-purity water system The FDA guidelines are dominating the aspect of microbiological conditions of water for injection and purified water systems that are used in the manufacturing of drug products. The guideline also covers the different types of high-purity water systems and their pros. and cons. Water system design as per FDA.
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Difference between QA and QC Department Quality assurance and Quality control both terms seem very similar in general but are very different in view of the roles they play in a company. In pharmaceutical manufacturing companies, both QA and QC have predefined roles and functions. These are not synonyms for each other but these two
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Top 10 pharma companies in India India has been self-dependent in the pharmaceutical sector for the last 40 years. Around 20000 pharmaceutical manufacturing companies were registered in India in 2002. Even then India used to export medicines to countries like Russia and America. In 2002 alone US $ 4 billion was exported to the US
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