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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.
Documentation Services: FAQ
Protocols
Raw Material Specifications
Finished Product Specifications
Final Reporting
Batch Records
Risk Assessments
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