Skip to main content
matrix pharma quality operation

Quality Operation

At Matrix Pharma we maintain a quality management system (QMS) while striving to meet international requirements and committing to continuously improve our laboratory standard.

Quality Assurance

Matrix Pharma has a well-built Quality Control department with highly specialized equipment HPLC, UV-Visible Spectrophotometer, FTIR, Particle Counter, Bio safety cabinet, Stability Climatic Chambers and other sophisticated equipment. To conduct testing & analysis through these specialized instruments we have a team of highly skilled and qualified professionals working dedicatedly to complying with the GLP & GDP to ensure release of the products of highest quality.

Our dedicated team ensures that each product meets and exceeds the expectations of our customers, consistently delivering uncompromising quality.

Where precision and perfection meet. Your satisfaction, our guarantee.

Quality Control

Quality Assurance is responsible to prepare systems for implementation of cGMP and to ensure the preparation, approval and execution of procedures & Qualification / Validation Protocols. Quality Assurance is responsible for qualification and certification of vendors of raw materials and packaging materials. Quality Assurance is also responsible for the finished product release and Annual product Review (APR). Quality Assurance is responsible to Conducts Technical Training programs for the employees’ awareness.