Icon-facebook Twitter Youtube Linkedin

Finished product testings– assay, impurity, dissolutions

Comprehensive Finished Product Testing for Release & Stability
GMP Analysis Across Tablets, Capsules, Creams & Liquids

Overview Service

Capzer Pharmaceuticals offers full GMP testing for finished pharmaceutical products, including tablets, capsules, liquids, creams, ointments, and suspensions. Our FDA-registered, DEA-registered lab ensures compliance with USP/NF, EP, JP, and client methods to support product release, stability, and commercialization.​​

Our Approach

We perform identity, assay, impurity profiling, dissolution, content uniformity, and degradation studies using advanced tools like HPLC-UV/PDA/MS, GC-FID/MS, dissolution apparatus (I & II), ICP-MS, and spectrophotometers. Protocols include compendial testing, method transfer/verification, and custom validation per ICH/FDA guidelines, delivering full data packages ready for regulatory submission.

Key Capabilities

  • Dissolution, residual solvents, elemental impurities, and nitrosamine testing.
  • Microbiology (sterility, microbial limits, endotoxin LAL per USP ).
  • Packaging integrity, particulates, and extractables/leachables studies.​

Benefits for Partners

Clients achieve faster time-to-market with reliable, traceable results from our cGMP-compliant facility, integrated with R&D and manufacturing. This supports ANDA filings, post-approval changes, and long-term partnerships for chronic therapies like Gabapentin and Empagliflozin generics.

Other Service

Need for help?

Our expert team is here to support you with reliable pharmaceutical testing, analytical solutions, and regulatory guidance. Whether you have a query or need a customized service, we’re ready to assist you at every step.

Contact Us