We have a modern and well-equipped Quality Control (QC) laboratory. InvaPharm’s QC lab tests all products for purity, safety and effectiveness. Products are released only after thorough analysis following stringent specifications, methods and procedures that comply with international guidelines. Our QC department has all necessary instruments for analysis of raw materials, 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:
The QC activities are managed through three sections:
Lab Equipment used for various testing:
Our QA (Quality Assurance) team crosschecks our manufacturing processes for compliance with written procedures, and 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. QA also monitors our lab procedures and instrument calibration protocols to ensure accuracy, precision, and reproducibility of our quantitative analyses.
Finished products are not released until QA completes the final inspection in accordance with written protocols.
A Certificate of Analysis is provided with each product to assure our customers of the reliability of products manufactured at InvaPharm. Each member of our team takes pride in their work. We guarantee that products manufactured by InvaPharm will pass any independent lab analysis. That’s our commitment to our customers.