Germany, France, and the UK lead the IVD market due to robust healthcare systems and government support. Key trends include personalized medicine, digital health, and the adoption of rapid and ...
Learn what the recently released CDSCO draft guidelines for medical device software within India actually mean.
New Delhi [India], October 24: Indian IVD manufacturers face growing regulatory hurdles under the EU IVDR. I3CGLOBAL provides strategic CE Marking support to small, medium, and large-scale ...
Biohope Announces Collaboration to Advance Immunobiogram Diagnostic Solution to Optimize Immunosuppression Therapy for ...
Medical Device Network on MSN
Biodesix and Bio-Rad expand collaboration for IVD assays development
Biodesix has expanded its collaboration with Bio-Rad for the development and clinical validation of in vitro diagnostic (IVD) ...
Despite the fresh set of guidelines, experts said that technologies like AI are increasingly being used in MedTech sector, ...
Expanding RPM to more health areas connects patients more seamlessly to healthcare professionals in between visits.
Biohope Announces Collaboration to Advance Immunobiogram Diagnostic Solution to Optimize Immunosuppression Therapy for Transplant Patients MADRID, ES / ACCESS Newswire / November 3, 2025 / Biohope, a ...
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 Regulation ...
CDSCO releases new draft guidelines aligning India's regulatory framework for medical device software with global standards.
Tempus AI, Inc. (NASDAQ: TEM), a technology company leading the adoption of AI to advance precision medicine and patient care, today reported financial results for the quarter ended September 30, 2025 ...
Upcoming free, educational webinars from Xtalks will feature topics on biomarkers, cell and gene therapy, clinical trials, commercialization & HEOR, drug discovery & development, drug safety, ...
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