More Lenient Guidelines May Inadvertently Lead to a Scarcity of Consented Samples Recently, no area has contributed more and increasingly complex layers to the bioethics debate than research employing ...

Dublin, May 02, 2018 (GLOBE NEWSWIRE) -- The "Contract Manufacturing in IVD: Market Analysis" report has been added to ResearchAndMarkets.com's offering. In vitro diagnostics markets rely on ...

HiMedia is dedicated to maintaining high safety, quality, and performance standards for in-vitro diagnostic products used in healthcare. This commitment significantly enhances the well-being of ...

In late July 2025, the UK government published its response to a consultation held between November 2024 and January 2025 about international reliance, UK Conformity Assessed (UKCA) marking and in ...

Dublin, Jan. 06, 2026 (GLOBE NEWSWIRE) -- The "Shanghai Kehua Bio-engineering Co Ltd (002022) - Product Pipeline Analysis, 2025 Update" has been added to ResearchAndMarkets.com's offering. Shanghai ...

Professional services consultancy, Procorre is urging the Medical Devices industry to take action ahead of the new ISO13485:2016 International Standard and MDD & IVD ‘Recast’ which become mandatory in ...

Taiwanese mobile health developer iXensor has obtained an undisclosed strategic investment from Rohto Pharmaceutical Co. to broaden the access to its core technology that transforms smartphones into ...

The UK Medicines and Healthcare products Regulatory Agency (MHRA) has published its responses to the consultation on Medical Device Regulations: Routes to market and in vitro diagnostic devices ...

The Central Drugs Standard Control Organisation (CDSCO), in collaboration with Indian Council of Medical Research (ICMR), has released the MedTech Mitra's handbook for innovators in the in-vitro ...

The "Contract Manufacturing of Medical Devices: Global Markets" report has been added to ResearchAndMarkets.com's offering. The global market for contract manufacturing of medical devices is estimated ...

The European Directive 98/79/EC on in vitro diagnostic medical devices, or IVD Directive (IVDD), became operational in June 2000. 1 It provides Europe with one single regulation for in vitro ...