The global In-Vitro Diagnostics (IVDs) Medical Device Market was valued at approximately USD 86 billion in 2024 and is projected to reach USD 135 billion by 2034, growing at a CAGR of 4.8% over ...

Learn how in vitro diagnostic (IVD) devices can comply with IVDR and Indian MDR standards, ensuring regulatory alignment, ...

Please use one of the following formats to cite this article in your essay, paper or report: APA. Molecular Devices UK Ltd. (2025, May 15). Modeling the intestinal epithelial barrier in vitro ...

The introduction of the Person Responsible for Regulatory Compliance (PRRC) role mandated under the Medical Device Regulation (MDR) 2017/745 and the In-vitro Diagnostic Device Regulation (IVDR ...

The PMS requirement applies to all UKCA- and CE-marked devices, like in vitro diagnostics (IVDs), glucose monitors, and ...

As the world of transfusion medicine evolves, so too does the complexity and capability of blood grouping and typing ...

While SaMD, referred to as “medical device software” or “MDSW” in Europe, is patentable, simply stating the use of AI in a technical field is usually not enough to secure a patent.

In recent years, the in vitro diagnostics (IVD) regulatory landscape in Europe has changed and we are now in the transition from IVD Directive 98/79/EC (IVDD) to In Vitro Medical Devices ...

New Post-Market Surveillance (PMS) regulations have taken effect across Great Britain, requiring medical device manufacturers to proactively monitor ...

A summary of preclinical evaluation methods for neuroendovascular devices, including in vitro techniques, 3D-printed vascular models, in silico simulations, and in vivo models.

In-Vitro Diagnostics (IVDs) Medical Device Market: 2025 to 2034Luton, Bedfordshire, United Kingdom, May 27, 2025 (GLOBE NEWSWIRE) -- Market OverviewThe global In-Vitro Diagnostics (IVDs) Medical ...