We have a modern and well-equipped quality control laboratory. InvaPharm’s QC lab tests all products for Identity, Purity, and Strength. We have a strict quality supplement manufacturing guarantee that ensures products are only released after thorough analysis. An analysis consists of following stringent specifications, methods, and procedures that comply with international guidelines. Our QC lab has all the necessary instruments for the analysis of raw materials, in-process products, finished products, packaging, and other materials used.


Raw ingredients, in-process materials, and finished products are tested for quality and conformity to written specifications at each stage of production. The QC team works closely with manufacturing so that all products meet or exceed established test specifications.

The QC department performs the following activities:

  • RM/PM analysis
  • Finished Products analysis
  • In-process Checks
  • Stability Studies (Ambient and Accelerated Condition)

The QC activities are managed through three sections:

  • Analytical Testing Laboratory
  • Wet Chemistry and Physical Testing Laboratory
  • Microbiological Testing Laboratory

Lab Equipment used for various testing:

  • ICP/MS
  • Particle Size Analysis
  • FTIR
  • Chemical Titration
  • pH Tester
  • Laminar Air Flow
  • Friability Tester
  • Hardness/Thickness Tester for Tablets
  • Hardness/Thickness Tester for Tablets
  • Total Organic Carbon Analyzer (TOC)
  • Dissolution and Disintegration
  • Moisture Analysis by KF Titration

Our Microbiological testing lab can test for the following:

  • TPC
  • Yeast
  • Mold
  • Coliforms
  • E-Coli
  • Salmonella
  • Streptococcus
  • And many more


Our QA (Quality Assurance) team crosschecks our quality supplement manufacturing processes for compliance. The QA team also interfaces closely with our customers to assure that we meet or exceed their quality requirements and product specifications. Through regular, in-house audits by the QA group, our production crew demonstrates conformity to cGMP requirements and assures the effective operation of InvaPharm’s operating system. The QA group also monitors our lab procedures and instrument calibration protocols to ensure accuracy, precision, and reproducibility of our quantitative analyses. A certificate of analysis is provided with each lot of products manufactured by InvaPharm. This gives you the assurance that the product meets quality specifications. Each member of our team takes pride in their work. We are committed to you, your brand, and your product.

We guarantee that products manufactured by InvaPharm will pass any independent lab analysis.