Method Development, Validation and Transfer

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  • Published date: April 1, 2019
    • Shirley, New York, United States

Method validation is essential for compliance with current good manufacturing specifications (CGMP) and good laboratory specifications (GLP). Analytical method validation (AMV) is the requirement of the biopharmaceutical industry for all methods used in the testing of raw materials, in-process materials, final containers and excipients. The development and validation of analytical methods is critical to drug development and access to reliable analytical data that you need to reach your next development milestone. The development and validation of methods can be complex, expensive, and labor-intensive. A full understanding of current regulatory expectations and related chemical methods, coupled with advanced instrumentation, is essential for the development of efficient, accurate and reliable analytical methods.

BOC Sciences has the latest advanced analytical instruments and top experts in all analytical areas. We can provide drug detection, environmental analysis, explosives investigation and identification of unknown samples even it is a very small amount of a substance.

https://www.bocsci.com/solutions/method-development-validation-and-transfer.htm

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