A London-based leading manufacturer of medical devices, specialized in devices used in Cardiac Surgery and Neuromodulation, approached Freyr for Regulatory support in product registration, license transfer and authorized representative services in Pakistan. The client already had its products registered in Pakistan but wanted to transfer the license of products and submit new product registration applications to extend its product portfolio.

How did Freyr manage to support the client while decoding the new Medical Device Regulations (MDR) 2017? Download the case study to decode.