Menu
×
×

Sign Up

Your Profile will be reviewed by Admin
EVENT DATES
Aug 2018
MoTuWeThFrSaSu
  12345
6789101112
13141516171819
20212223242526
2728293031  

Venue

TBD
Google Map

EU MDR 2017/745: Optimizing Clinical Evaluation Reports within the Medical Device Lifecycle
This event profile is claimed and maintained by the event organizer.
More

Online Event

Attendees

-

Exhibitors

-

Register

FREE

Overview

Event website:https://bit.ly/2zK2vBJ

In this webinar, NAMSA’s Manager of Medical Writing and Regulatory Services (EMEA), will examine the requirements listed in the MDR and MEDDEV 2.7/1 Rev 4, and discuss why device manufacturers shall not consider the CER a mandatory document for NBs or authorities, but rather as a crucial tool for a smooth transition for MDR and beyond.

Agenda

Aug 7   

In this webinar, NAMSA’s Manager of Medical Writing and Regulatory Services (EMEA), will examine the requirements listed in the MDR and MEDDEV 2.7/1 Rev 4, and discuss why device manufacturers shall not consider the CER a mandatory document for NBs or authorities, but rather as a crucial tool for a smooth transition for MDR and beyond.

Keynote Speakers

Paul Malinovski

Manager of EMEA

NAMSA

Paul Malinovski is based in Berlin and serves as NAMSA’s Manager of EMEA Medical Writing and Regulatory Services. Prior to joining NAMSA, Paul worked at UL-MDT as Managing Director (MDT) and Regional Operations leader (UL). Mr. Malinovski has also held the position of Senior Regulatory Affairs Manager at Zimmer Biomet where he was responsible for global regulatory affairs on bone cements, including combination products. Paul has a wealth of expertise in global regulatory affairs, including the geographies of Europe and Russia, in addition to Medical Writing for CERs per MEDDEV.

SERVICE PROVIDERS

MORE events +

I Want to


Send me discounts and offers from hotels nearby
By Signing up you agree to User Agreement and Privacy Policy
I want to list my services