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.



Raw Material Specifications

Finished Product Specifications

Final Reporting

Batch Records

Risk Assessments