How to reply whenever the Notified Body, the Certifying Body or the Competent Authority request corrections, solutions and changes during the certification or MDR (UE)2017/745 inspection?

How to overcome objections or requests that block the process?

YOU CAN FIND THE ANSWER TO THESE QUESTIONS HERE:

MDG 2022 – MedGenerAction

September 29th, 2022

Bologna (Zanhotel Europa) or streaming

MedGenerAction is the annual Summit directed to professionals dealing with Regulatory Activities applied to Medical Devices and this VIII edition aims to provide winning response strategies to the most challenging non-compliance released in the certification and MDR control phase.

Under the guidance of Thema experts who live real and concrete experiences every day in the management of MDR practices, you will get to know the best methods to achieve the desired objectives.

MD24 IS THE BRAND BY THEMA FOCUSED ON QUALITY&REGULATORY TRAINING TO MEDICAL PROFESSIONALS.

THEMA IS THE COMPLIFE COMPANY SPECIALIZED IN STRATEGIC REGULATORY CONSULTING FOR MEDICAL DEVICES (MD) AND IN-VITRO DIAGNOSTIC DEVICES (IVD).

COMPLIFE. COMMITTED TO SCIENCE, COMMITTED TO YOU.