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.
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
Read More >
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…
Read More >
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.
Read More >
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.
Read More >
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.
Read More >
As clinical trial designs become more and more complex, processing and tracking site payments is also becoming more challenging and complex.
Read More >
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.
Read More >
Numerous factors are changing the way clinical trials are conducted. Increasingly complex trial designs, global patient groups, and decentralized trial models have significantly impacted how trial information is tracked and managed. These factors have also influenced how clinical professionals manage trial supply and inventory.
Read More >
Adaptive trial designs emerged as a means to improve clinical trials based on all available information. High failure rates and increasing costs have driven the industry toward adaptive trial designs….
Read More >
Introduction Real-Word Data (RWD) and Real-World Evidence (RWE) are acronyms that have been thrown around the industry for some time. As healthcare, life sciences companies and regulators look at the potential research opportunities that stem…
Read More >