The Quality Assurance Department reviews every aspect of the manufacturing, from raw materials to final shipping, and makes sure that Good Manufacturing Practice are followed. Aseptic Process Simulation are periodically carried out in order to guarantee that the Drug Product is aseptically produced by qualified operators in qualified suites.
The release of the final Drug product is assured by a Qualified Person or its deputy, that certifies your Investigational medicinal products (IMPs) for use in clinical trials before shipping.
“The principles of quality, standardization, and process robustness guide us in ensuring the safety of your product for patients”