MDCG 2024-3 – Guidance – Russell Regulatory Consultants Ltd

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Russell Regulatory Consultants Ltd

ABHI UK Healthtech Conference
About Us
April Medical Device Regulatory Updates
Artificial Intelligence
Basket
Blog
Blogs
British Medical Association Clinician Conference
Checkout
Clinical Evaluation
Clinician Bank
Clinician Bank Service Launch
Contact
Cosmetics Regulation
Did You Know That The IDAP Programme Deadline Was The 29th October 2023?
EU Regulations and Guidance
European Commision MDR Update
Extension Of The MDR transition Period
February Medical Device Regulatory Updates
FutureScot Health and Transformation 2024 Conference
Guidelines For Manufacturers Have Been Updated
Home
Insights from MedTech Innovations Expo 2023
International Regulations and Guidance
Interview with Bridie Houlihan of the Female Health Founders magazine
January Medical Device Regulatory Updates
July Medical Device Regulatory Updates – Copy
June Medical Device Regulatory Updates
March Medical Device Regulatory Updates
May Medical Device Regulatory Updates
MDCG 2024-3 – Guidance
MDCG Draft: Equivalence Guidelines for Class III and Implantable Devices
Med-Tech Innovation Expo 2023
Med-Tech MTI News Magazine
Medical Device Regulatory Services
MedTalk Podcast Feature
MHRA Eases Medical Device Qualification: New Guidance Available!
MHRA Proposes 2024 Updates to Post-Market Surveillance
My account
New Dedicated Resource For Reviewing Technical Documentation
New MDCG 2022-11 Rev1 Position Paper Published
New Office In Glasgow
New partnership with St Ogilvie High School
News
Opening New Glasgow Office
Privacy Policy
Quality Management Services
Regulatory Intelligence Blog
Russell Regulatory are now officially offering IVDR services
Russell Regulatory Consultants is now an accredited Living Wage Employer!
Russell Regulatory Consultants Turns 5 years Old
Sample Page
Services
Shop
Shop
Sponsors of ABHI Conference, London
Team NB Urges Swift MDR Transition
Team-NB’s Analysis: MDR Transitional Timelines & Challenges in Notified Body Capacity
Thank You
The EtO Emissions Ruling for Medical Devices in the USA
Top Tips For Literature Searches
TOPRA Scotland Event Insights with Edwin Lindsay
UK Extends CE Marked Medical Devices Acceptance
UK Responsible Person
UKCA Marking News- Changes to Post- Market Surveillance Anticipated
Ways You Can Work With Us
We are now part of the TOPRA – The Organisation for Professionals in Regulatory Affairs
We Now Offer Medical Device Training Courses
We Now Offer Referral Fees
Welcoming Stephanie To The Team
Whitepapers

MDCG 2024-3 – Guidance

March 2024

MDCG 2024-3 was released yesterday on the content of the Clinical Investigation Plan for clinical investigations for medical devices.

https://lnkd.in/dH8aCyGn

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