All of the finished dosage forms we use are of the highest quality and were purchased from a trustworthy manufacturer.

Ensuring Quality system through inspection, Documents review like Factory Licence, Valid GMP / GLP Certificates and Manufacturing License issued by FDA.

Assessment of Manufacturers through background of Manu Responsibility_dvfacturers, Site Master File, No of Employees, Manufacturing Equipment’s / Instrument Design, Qualification, Calibration, Manufacturing / Packaging and Testing facility etc.

Assessment of Manufacturer through Quality Management system implemented at manufacturing site like Review system, Quality assurance Responsibility_dvcontrol, Training of personnel on GMP / GLP understanding, in process QA control during manufacturing and Packaging of Drug products and Technical / Quality agreement.

Ensuring that any batch supplied to RD Group has a GMP statement, certificates of analysis and batch documents from the manufacturer.

Testing of Products through other accredited Contract testing laboratories to enhance and build up confidence and cross checking of product quality and efficacy.

Following good distribution procedures and ensuring storage of drug products according to the prescription label's prescribed storage conditions.