PIER is delighted to announce details of the first EIPG/PIER webinar of 2018 on the topic of 'Insight into New Medical Device Regulations in the EU' on Tuesday 13th March 2018 at 4pm (GMT).
Overview of Webinar:
EU legislation has been updated for both Medical Devices and In-vitro Diagnostic Medical Devices with major changes in the requirements such as clinical evaluation and performance testing. In parallel, Quality System Standards have been updated. Tightening regulations give more challenges for Medical Device companies throughout Europe. After attending this webinar, participants will be able to:
- Define what is a medical device.
- Recognise the reasons for the two new Regulations.
- Understand the key aspects of the new legislation.
About the Speaker:
Petra Lehtinen MSc (Pharm) is Senior Regulatory and Quality Management Specialist at Biocodex PHAME (Pharmaceutical and Medical Services).
To Join the Webinar:
Please register for the event by filling out the form at https://docs.google.com/forms/d/e/1FAIpQLSdUBoelICCL0i5T_HgoF7K9Up1Ycxp3GimOcLuzfxyECdamQ/viewform. Further instructions will then be sent by e-mail. Attendance is free to current PIER members.