Classification of Medical Devices.
12/10/2021
October brings in clarification on the classification of different medical devices under the EU MDR.
75% IVDs may Lack IVDR Certification!
21/9/2021
MedTech Europe warns IVD manufacturers might not be able to certify their product before the deadline.
17/9/2021
Presenting Med-Di-Dia Friday Weekly Run Through for 17th September 2021
All things MedTech and Regulatory
8 Challenges Affecting Medical Devices
7/9/2021
Top challenges affecting Medical Device Manufacturers.
Clinical Trials Information System (CTIS)
5/8/2021
The EU Clinical Trials Information System (CTIS) will go live on 31 January 2022 - why does this matter to MedTech? Read on
Tech Supporting Medical Services!
3/8/2021
Read about how tech is supporting counselling services for children.
Med-Di-Dia's Presentation On Helix!
15/7/2021
07th July, Med-Di-Dia and its partners presented insights as a part of the ON Helix Innovations workshop. Read more…
Latest Guidance on UDI by USFDA
8/7/2021
Just in: Latest Guidance issued by USFDA. Find out more here…
Med-Di-Dia Takes Part in Innovation Workshop with ON Helix
5/7/2021
The One Nucleus community organises ON Helix Innovation workshops, and this time, Med-Di-Dia is participating with its Partners. Read More
1/7/2021
Started in 2019 - Embraced the Pandemic and now we are here!
Read our celebrations!
EU MDR and the United Kingdom.
29/6/2021
With complex developments in the regulatory framework, it is vital to stay up-to-date. Read on to know more about the EU MDR and the United Kingdom.
