A multinational pharmaceutical company approached Freyr for Regulatory assistance with audit services for conducting bioequivalence studies. The scope of the project included auditing more than 15 Clinical Research Organizations across India. The client was facing multiple challenges with the project as there was unavailability of documents during the audit and the timeline was short.

Read through the case study to decode how Freyr managed to conduct 120+ studies at multiple client locations in the specified time and increased the savings up to 40%.