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FREE ON-DEMAND WEBINAR 12th Dec, 2024 4:00 PM - 5:00 PM GMT

Technical Documentation under the EU MDR 2017/745

Technical Documentation under the EU MDR 2017/745

Join us on Thursday, December 12th 2024, from 4-5pm GMT, where Comply Guru’s newest team member Orla Keane will discuss Technical Documentation under the EU MDR 2017/745. The discussion will be moderated by Michelle Keane.

This Webinar will discuss key topics including:

Best Practices & Pitfalls to avoid on MDR Technical Documentation
A Notified Body and Industry Perspective
Structure of Submission
Importance of Clear Content
Attention to detail in relation to Consistency
Q&A

Register for FREE to gain access to this Webinar (Live Event).

Register for free

Orla Keane

Orla Keane

QA/RA Instructor

Orla is a highly respected Medical Device QA/RA Professional with over 20 years experience gained in roles in industry, consultancy, notified bodies and competent authorities. During her illustrious career where she has worked with the Irish Medicines Board, HPRA, NSAI (Notified Body) as well as various Senior Quality and Regulatory Roles, she brings a wealth of knowledge & experience to Comply Guru.

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CQI & IRCA Approved Training Provider

CQI & IRCA Approved Training Provider

Offering certified courses since 2019

Exemplar Global Recognized Training Provider

Exemplar Global Recognized Training Provider

Offering certified courses since 2020

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