FDA 21 CFR Part 11 and the importance of regulatory compliance in GMP and GLP labs
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FDA 21 CFR Part 11 and the importance of regulatory compliance in GMP and GLP labs
The regulations for food and drugs in the United States, described in Title 21 of the Code of Federal Regulations (CFR), are critical in ensuring safe and ethical drug administration. Whether you are an academic institution, a government agency, or a pharmaceutical company, you have to adhere to these rules at each step of the […]
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