The evolving EU MDR and IVDR present key opportunities for companies to enhance compliance strategies, engage with notified bodies, and optimize market access. Staying informed and proactively ...

Registrar Corp aims to integrate its network with CMC’s offerings to help medical device companies in bringing products to ...

Medical device makers use AI to turn EU regulatory challenges into competitive advantages via supply chain optimization.

Learn what the recently released CDSCO draft guidelines for medical device software within India actually mean.

SeeTreat announced today that its offline adaptive radiotherapy software, ART.1, has received CE Mark certification under the European Union Medical Device Regulation and is now available for clinical ...

Here are three important regulatory changes affecting parenteral packaging that pharmaceutical companies need to be aware of ...

Hohenstein Medical ? a division of Hohenstein Laboratories and a leading provider of testing, research and certification services for medical devices ? has hired Katie Brinkman as its biocompatibility ...

Third Quarter 2025 Financial and Operating Results Revenue was $14.7 million for the three months ended September 30, 2025, an increase of $1.3 million, or 10%, over the three months ended September ...

A live audio webcast of the conference presentation will be available online at the investor relations page of the Company’s website at ir.cvrx.com. CVRx is a commercial-stage medical device company ...

CDSCO updates list of Class A non-sterile and non-measuring devices: Gireesh Babu, New Delhi Tuesday, November 4, 2025, 08:00 Hrs [IST] The Central Drugs Standard Control Organisa ...

Hyaluronic acid (HA) products are widely used in both medical and cosmetic fields due to their excellent moisture-retention, ...

The medical device industry landscape is evolving rapidly, driven both by regulatory changes and the quest for innovation. The new European Medical Device Regulation (EU MDR) and its implementation ...