EU Health Technology Assessment: public consultation and Joint Scientific Consultations now open
The implementation of the EU Health Technology Assessment (HTA) [...]
Sterile gloves, sterile devices and patient transport equipment: what changed in 2025
In 2025, the European Commission introduced a new set [...]
6 common mistakes in MDR technical documentation (and how to avoid them)
Creating technical documentation for MDR compliance can be challenging. [...]
CDSCO cosmetic product registration cancelled: what this case teaches manufacturers
On May 20, 2025, the Central Drugs Standard Control Organisation [...]
Legacy devices: no need to update the label with a UDI-DI
If you are still placing legacy medical devices on [...]
PRRC MDR IVDR: role, requirements and compliance duties
What is the role of the PRRC? The person [...]
What happens after May 26, 2025? UDI-DI compliance and market consequences
As of May 26, 2025, manufacturers of: class I [...]
CE marking for Class I medical devices: Can I self-certify my product?
Many manufacturers assume that Class I medical devices can [...]
How to register a medical device or IVD in Saudi Arabia: SFDA registration process explained
Getting started with SFDA registration If you plan to [...]
New MIR 7.3.1 form mandatory from November 2025
The European Commission has released the new Manufacturer Incident [...]
