The client was a leading Indian pharmaceutical manufacturer looking for Regulatory support in filing DMF submissions with 100% accuracy. There were several challenges in the project such as maintaining the lifecycles of multiple products and strict timelines. Freyr identified the need for tracking versions of frequently changed documents and filing them in the eCTD format. Freyr deployed several full-time employees to offer continual support and filed the submissions to the CDSCO for the DMF requests.
Know more about how Freyr overcame multiple challenges and offered Regulatory support to enable the client to file the DMF submissions with 100% accuracy in stringent timelines.