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 ...

The Central Drugs Standard Control Organization (CDSCO) has released a draft guidance document on the conduct and regulation of Medical Device Software (MDSW) under the Medical Devices Rules (MDR), ...

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 ...

Selenis launch of Selcare CE 500 delivers high performance and RIC1 waste stream compatibility for sustainable Healthcare ...

VUNO, Kakao Healthcare, Skylabs, and Remidio advance into Europe with partnership deals and regulatory approvals for AI in ...

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 ...

Alife Health, a health tech company advancing the future of fertility care with artificial intelligence, today announced that Embryo Predict™, its AI-powered embryo selection tool, has received CE ...