Manufacturing of biological products needs strict as well as careful monitoring, quality control, and documentation of all aspects of the complicated process including regulatory as well as in house records. Among these, the documentation, regulatory formalities are time consuming and need a rigorous check.

We at Raj Pharma Consultancy gives you all the support by helping you for regulatory filing. Our team helps you to apply for the licence keeping in view of the latest requirements of the cdsco, including post approval changes, if any.

We help you partner with reputed CRO’s for successful filing of application for the purpose of conducting Clinical Trials, etc., and after getting the trials completed in time, we arrange for the fast tracking the final approval from the office of cdsco.