Post-market surveillance: FDA-approved proactive medical devices reporting | HCL Technologies

Post Market Surveillance-Proactive Medical Devices Reporting

Proactive post-market surveillance is an important part of a Medical Device lifecycle. This white paper actively discussed about all the proactive approaches that can be done on medical device to avoid complaints, recalls and market withdrawals.

Proactive post market surveillance plays a vital role in the PMS of any Medical device. If implemented properly, it helps the manufacturer to improve their product performance. The additional advantage for manufacturer is not only it helps for product improvement and meeting the regulatory requirements, It enables to proactively reduce / eliminate the future complaints from occurring and so the Product recalls, Customer dissatisfaction.

Download the whitepaper