Paul Piscoi
Latest contributions
Update on the regulation of high-risk medical devices: a transatlantic perspective
25 Jun 2020 – From PCR e-Course 2020
Watch this session if you want to get an update on new developments in the regulation of high-risk medical devices in Europe and the USA and to learn about opportunities for physicians to become more involved in the regulatory environment.
This session was originally presented during PCR...
The future of medical device regulation in the European Union
New EU regulations on medical devices will come into force in 2020. Giulio Stefanini, Robert Byrne and Paul Piscoi discuss how new regulation is needed “to reflect the changes in the field over the last decades” and outline what this will mean for the safety of...
Optimising the generation and regulatory application of clinical evidence in the European Union and the United States
22 May 2019 – From EuroPCR 2019
Consult this session to discover innovative approaches for collecting and utilising clinical evidence, and learn more about how to conduct efficient clinical research to support marketing approval in the European Union, the United States, or regions dependent on the CE mark or FDA approval.
