Medical Devices and Clinical Evaluation
Understanding the clinical evaluation requirements for the medtech industry
The most significant regulatory changes coming along with the EU Medical Devices Regulation 2017/745 (MDR) and MEDDEV evolutions affects the clinical evaluation of medical devices.
This course gives participants an overview on the requirements for the clinical evaluation of medical devices and the impact of the MDR and guideline documents on clinical activities. The course further describes how to prepare the new requirements from a clinical perspective including the MEDDEV 2.7.4/1 on clinical evaluation and the MEDDEV 2.12/2 on post market clinic follow up. The training will allow participants to obtain a clear understanding of the regulatory requirements and will give hands on insight on how to achieve compliance.
Date: 16 April 2019
Time: 9 am – 6:00 pm
Venue: Barcelona, Spain
Cost: Early bird: € 850* (until 18-03-2019)
Ordinary: € 960*
Freelance – Academy – Public Administration: € 460*
* For Italian companies: + 22% VAT
The fee includes: tuition, teaching materials, lunches and coffee breaks, office assistance, attendance certificate
Complete booking and payment at this link and use code MVA1908 to book and receive 15% off.
For any further question feel free to contact Mara Claudia Algarotti firstname.lastname@example.org