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Clinical Evaluation of European Medical Devices: The Clinical Evaluation Report (London, United Kingdom - June 3-4, 2020) - ResearchAndMarkets.com

December 2, 2019

DUBLIN--(BUSINESS WIRE)--Dec 2, 2019--

The “Clinical Evaluation of Medical Devices: The Clinical Evaluation Report” conference has been added to ResearchAndMarkets.com’s offering.

Cover all the aspects of clinical evaluation in line with the European medical device regulations and applicable guidance documents

Course Overview

Why you Should Attend

This two day course will cover all the aspects of clinical evaluation in line with the European Medical device regulations and applicable guidance documents. The course will provide you with the tools and skills you will need to produce a high quality clinical evaluation report for all your medical devices. You will understand the detail of what clinical data is needed, how to collect it, analyse it and produce a clinical evaluation report that is acceptable to the Regulatory Authorities and Notified Bodies. You will learn how the process fits into the development of a medical device and also the post market aspects of clinical evidence. The course includes case studies and template documents which you will be able to utilise to produce your own high quality clinical data evidence documentation.

Who Should Attend:

Agenda:

Programme Day 1

Objectives and overview

What is a clinical evaluation?

Why and when is it necessary to conduct a clinical evaluation?

Who and what is involved in the clinical evaluation process?

Workshop : Bringing it together

What regulations govern clinical evaluations and what guidance documents should clinical evaluations be conducted to?

Quiz

Q & A and wrap-up of day one

Programme Day 2

Review of day one, introduction to the day, objectives and overview

Documentation necessary for conducting a clinical evaluation

The literature review process

The Clinical Evaluation Report (CER)

What is state of the art and how to conduct a risk benefit assessment of the data?

Impact of the Medical Device Regulations (MDR)

Quiz

Q & A and wrap up

For more information about this conference visit https://www.researchandmarkets.com/r/qy7nhh

View source version on businesswire.com:https://www.businesswire.com/news/home/20191202005501/en/

CONTACT: ResearchAndMarkets.com

Laura Wood, Senior Press Manager

press@researchandmarkets.com

For E.S.T Office Hours Call 1-917-300-0470

For U.S./CAN Toll Free Call 1-800-526-8630

For GMT Office Hours Call +353-1-416-8900

KEYWORD: UNITED KINGDOM EUROPE

INDUSTRY KEYWORD: EDUCATION TRAINING HEALTH MEDICAL DEVICES

SOURCE: Research and Markets

Copyright Business Wire 2019.

PUB: 12/02/2019 08:11 AM/DISC: 12/02/2019 08:11 AM

http://www.businesswire.com/news/home/20191202005501/en