Mednet offers a unified clinical trial platform combining EDC, RTSM, CTMS, eConsent, ePRO, eTMF, safety, and intelligent automation — empowering sponsors and CROs to accelerate study startup, enhance data quality, and maintain continuity across all stages of clinical development.
Examining the challenges, progress, and significance of clinical research in honor of Rare Disease Day, February 29, 2024. Rare disease trials are clinical studies designed to evaluate the safety and…
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Clinical research teams require different types of support to be successful and to get the most from
their technology investment while still maintaining
quality and compliance. Each project is unique, each research team is unique, and each have unique requirements to achieve success.
The Clinical Data Acquisition Standards Harmonization (CDASH) was designed to standardize data, with recommended data collection fields, implementation guidelines, best practice recommendations and regulatory references. CDASH’s consistent approach to collect…
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In the highly complex and rapidly evolving world of clinical trials, a strong partnership between a contract research organization (CRO) and its technology partner is critical to success
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It’s no secret that clinical trial technology plays an increasingly prominent role in research. New advances in eClinical solutions are changing the face of the industry. But how exactly are…
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In celebration of National Nurses Week, we interviewed Sadie Samson, a Mednet Project Manager who is also a nurse. Sadie was a client before joining the Mednet team, so she brings a unique perspective and a wealth of relevant experience to her clients’ projects.
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Ophthalmology studies are unique in many ways. Over the years, the Mednet team has supported research across the world and hundreds of studies in ophthalmology, related diseases and treatments have been conducted on the iMednet platform.
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Our new partner story details our relationship with one of our long-term CRO partners, SDC, and how we’ve collaborated to evolve the iMednet platform to meet the evolving requirements of clinical research studies and the needs of research teams around the world.
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As clinical trial designs become more and more complex, processing and tracking site payments is also becoming more challenging and complex.
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With remote participation by staff and participants on the rise, efforts have focused on improving the patient experience and effectively engaging patients as active participants.
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