•The necessity of the risk management plan (RMP) has been studied before the launch of the medical device and medicinal product. <br />•Risk management documents/plan for medical device is done and verified through FDA QS regulations and ISO 14971. <br />•For medicinal products the risk management documents/plan is achieved by <br />•If more than one medicinal product is studied, article 14(2) of Regulation (EC) No 1394/2007 provides a layout for RMP for such advanced therapy medicinal products (ATMP) <br /> <br />To Continue reading : https://bit.ly/3e1harA <br /> <br />Contact us; <br />website: https://bit.ly/2W1nV6r <br />Email: sales.cro@pepgra.com
