Our GMP-certified QC Release Testing services provide full analytical support for the release of pharmaceutical, nutraceutical, and chemical products. We ensure that every batch meets regulatory, specification, and quality requirements prior to market distribution. All testing is performed in a GMP-compliant environment using validated methods, state-of-the-art instrumentation, and scientifically robust data practices.

We test across a wide range of dosage forms — including tablets, capsules, powders, liquids, suspensions, creams, and gels — applying industry-standard methods and client-specific protocols as required. Our experienced analysts and QA team ensure timely and compliant data delivery to support product release and regulatory submissions.

Comprehensive Testing Capabilities Include:

• Chemical Testing

  • Quantitative determination of active ingredients and impurity profiling

  • Dissolution Analysis

• Physical & Chemical Testing

  • Appearance, pH, specific gravity, viscosity

  • Uniformity of dosage units and weight variation

  • Moisture content, loss on drying, and other stability-indicating tests

• Analytical Techniques & Instrumentation

  • High-Performance Liquid Chromatography (HPLC)

  • Ultraviolet/Visible Spectrophotometry (UV-Vis)

  • GC, FTIR, TOC, KF, and other validated major techniques

  • Chromatographic and spectroscopic methods tailored to formulation type

• Product Types Supported

  • Pharmaceuticals (API and finished products)

  • Nutraceuticals and dietary supplements

  • Specialty and industrial chemicals

• Regulatory & Quality Assurance

  • GMP-certified laboratory operations

  • Comprehensive documentation packages for audits, submissions, and release

  • Data integrity, traceability, and compliance with global quality standards