FDA 21 CFR Part 211
We offer solutions that ensure compliance with the standard.
The challenge
The Food and Drug Administration’s (FDA) standards for Title 21 of the Code of Federal Regulations (CFR), also known as the FDA 21 CFR, provide a clear and concise set of regulations.
A specific focus of FDA 21 CFR part 211 is current good manufacturing practices for finished pharmaceuticals.
Do you need more information about the requirements your company must meet regarding the regulations in force in the sector?
Oqotech's team has over 10 years of experience in the pharmaceutical, biotechnology and food industry. We guarantee that the organization complies with legislation. Leave your details and we will contact you to offer you more detailed advice.
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