Chemistry

Pace Analytical Life Sciences offers analytical chemistry services for the qualitative and quantitative assessment of Active Pharmaceutical Ingredients (API), In-Process Materials and Finished Products. We follow client-supplied methods, compendial methods or methods that we have developed and validated for our clients. Client-supplied methods are typically transferred following a specific method transfer protocol. Compendial methods are verified according to a verification protocol.

This department has a broad-based working knowledge of many dosage forms. We have tested classic oral dosage forms (tablets, capsules) to liquid, topical and semi-solid dosage forms. We also have a wealth of knowledge working on specialty dosage forms such as transdermal systems and aerosol products.

Pace Analytical Life Sciences offers the following analytical chemistry services to the Pharmaceutical industry:

Method Development/Method Validation
Method Transfer/Method Verification
Stability Testing and Storage
Raw Material Testing (USP/NF, EP, JP)
Quality Control Release Testing
Dissolution
Extractable/Leachable Testing
Residual Solvents
Remedial/Retrospective Method Validation

Microbiology Services

Pace Analytical Life Sciences provides cGMP compliant analytical chemistry services following compedial methods, client-supplied methods or methods that have been custom-developed to meet client specific requirements.