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Documentation Services

The pharmaceutical industry is one of the most heavily regulated industries in the world with oversight agencies existing in nearly every country in the world.


Documentation for a pharmaceutical manufacturer is monumental and errors can be costly.

BRS is an ethical, competent, and experienced partner who can aid in navigating the landscape associated with GMP/GLP documentation and ensuring scientific integrity.

 

Protocols

Raw Material Specifications

Finished Product Specifications

Final Reporting

Batch Records

Risk Assessments

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