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How the right technology and tools can accelerate progress in rare disease clinical trials

August 29, 2023

Biopharmadive Although diseases such as Ehlers-Danlos syndrome, Sanfilippo syndrome and Hemophilia are considered rare, their impact looms large. Rare diseases, defined as occurring in fewer than one in 2,000 individuals, affect more than 300 million people across the globe, and most have considerable unmet medical needs. The need for more research into rare diseases is clear, but researchers face significant challenges, […]

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Essential considerations for a successful submission under EU CTR

August 29, 2023

International-Biopharma The European Union Clinical Trials Regulation (EU CTR), which came into force in January 2022, was the biggest change to EU medicinal product legislation since 1995 when the European Medicines Agency (EMA) and the centralised procedure for marketing authorisations were introduced. The EU CTR presents fundamental changes for clinical trials in all 30 countries […]

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How AI infused solutions can improve clinical workflows

August 29, 2023

Medtech Dive Technology has transformed healthcare, particularly in the areas of medical documentation and common clinical tasks. With conversational AI, ambient AI and generative AI, the industry has been propelled forward, enabling new functionalities and infusing healthcare experiences with intelligence. These advancements are contributing to improved patient care and enhanced clinician-patient experiences, making it possible […]

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EUCROF Code of Conduct in a Nutshell

June 22, 2023

Webinar – June 28, 2023 After several years of work, the European Federation of CROs (EUCROF) is close to the finalisation of a GDPR Code of Conduct for clinical vendors. This Code sets out the practical terms of compliance with the GDPR, in the specific field of clinical research and particularly Clinical Research Service Providers. […]

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