Regulatory Affairs Professionals Society (RAPs)

RAPS and TOPRA have joined forces to deliver a workshop to help regulatory professionals understand the impact of the EU’s new MDR on combination products. Read more


With Brexit looming, Paul Brooks, executive director, Regulatory Affairs Professionals Society (RAPS) discusses how medical device companies should respond to the EU's new Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). Read more


Paul Brooks, executive director at the Regulatory Affairs Professional Society (RAPS) discusses how Notified Bodies are preparing as they transition to the new regulations and the wider impact that this has on the medical device sector. Read more


Paul Brooks, Regulatory Affairs Professionals Society (RAPS), discusses the impact of European Medical Device Regulation on currently marketed medical devices and offers guidance for manufacturers. Read more