Skip to content
CMS MedTech
  • Home
  • About
  • Services and Free Resources
    • Outsource Personnel
    • Technical Documentations
    • Coordination for testing
    • Quality Management System
    • Audit
    • External Audit
    • Medical Device Registration and Local Representation
    • Training
  • Medical Device Regulatory Updates
  • Contact

Month: May 2024

EXTENSION OF THE MDR TRANSITIONAL PERIOD AND REMOVAL OF THE ‘SELL OFF’ PERIODS

Posted by By cmsmedtech May 31, 2024Posted inCE
Q&A on practical aspects related to the implementation of Regulation (EU) 2023/607 amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards the transitional provisions for certain medical devices and in…
Read More
Recent Posts
  • Medical Device Registration in Thailand

    Medical Device Registration in Thailand

    January 9, 2024
    Authority for Medical Device Thai FDA Medical Device Control Division …Read More »
  • Medical Device Registration Vietnam (updated 2023)

    Medical Device Registration Vietnam (updated 2023)

    April 28, 2023
    Authority for Medical Device Department of Medical Device and Constructions …Read More »
  • Medical Device Registration in UK

    Medical Device Registration in UK

    January 27, 2023
    Authority for Medical Device Manufacturers must register their devices with …Read More »
  • Medical Device Registration in New Zealand

    Medical Device Registration in New Zealand

    January 13, 2023
    Authority for Medical Device Medsafe Medical Device Definition Legal Definition …Read More »
  • EU Authorised Representative

    EU Authorised Representative

    January 13, 2023
    In which cases do you need to assign the EU …Read More »
Archives
  • May 2024
  • January 2024
  • April 2023
  • January 2023
  • January 2022
  • November 2021
  • October 2021
  • September 2021
  • July 2021
  • June 2021
  • May 2021
  • April 2021
  • March 2021
  • February 2021
  • December 2020
  • November 2020
  • October 2020
  • September 2020
  • August 2020
  • July 2020
Categories
  • Armenia
  • Asean
  • Australia
  • Bangladesh
  • Belarus
  • biological evaluation
  • Brazil
  • Cambodia
  • Canada
  • CE
  • cer
  • Colombia
  • common specifications
  • Covid-19
  • csdt
  • EC REP
  • eu doc
  • IMDRF
  • India
  • Indonesia
  • ISO 13485
  • Japan
  • Kazakhstan
  • Kyrgyzstan
  • Malaysia
  • Mexico
  • Myanmar
  • New Zealand
  • Pakistan
  • Philippines
  • pms
  • Russia
  • Saudi Arabia KSA
  • Singapore
  • Taiwan
  • technical documentation
  • Thailand
  • UAE
  • udi
  • UK
  • Ukraine
  • Uncategorized
  • US
  • Vietnam
Email: cmsmedtech@compliancems.com.au | Copyright 2025 — CMS MedTech. All rights reserved.
Scroll to Top
Open chat
1
WhatsApp
Hi this is Kit. Please feel free to ask us any questions via short messages. We usually reply within a few hours.