Services Medical Devices Post Marketing
Post Marketing
Post-Market Surveillance (PMS) Systems and Planning is a key element for continued compliance of the device to the regulations.
Post Market Clinical Follow Up Studies/ Post Market Performance Follow Up Studies
PMCF and PMPF are both key elements for continued compliance with Regulations. Strategy for PMCF/PMPF will depend on the device type and the organisational set up. DLRC are able to create a strategy which is compliant to the requirements and bespoke for each organisation to carry out these studies effectively.
Vigilance/ Periodic Safety Update Report
Vigilance reports and PSURs are mandatory activities under particular regulations and completion of the reports and forms to remain compliant can be achieved by DLRC in order to assist our clients.
