SFLs Managing Director Invited to Speak at World Medtech Forum
Summary
Basel, Switzerland, September 22, 2012 --( “The existing EU regulations for medical devices were drafted 20 years ago and so changes to address the current environment have become necessary.It is important that the medtech companies very closely monitor changes and implement measures ensuring timely compliance with the new requirements,” commented Shayesteh.She has been a member of the Program Committee of DIA EuroMeeting for 2011, 2012 and 2013 leading the Theme Drugs, Devices, In Vitro Diagnostics and their Combinations.Shayesteh’s presentation will be entitled “How to prepare for medtech regulatory changes – Insights into recent developments at the European Commission.” During Shayesteh’s talk, the audience will learn about the current medtech regulatory framework in Europe, anticipated changes by the Commission and how they might impact the industry.“The existing EU regulations for medical devices were drafted 20 years ago and so changes to address the current environment have become necessary.It is important that the medtech companies very closely monitor changes and implement measures ensuring timely compliance with the new requirements,” commented Shayesteh.Shayesteh is the Managing Director and founder of SFL.