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Reading Time: 4 minutesThis blog was authored by Marc Kaufman, Senior Product Director, Product Management at Medidata. Planning, implementing, and managing technology are important considerations during the trial planning phase. Also essential is incorporating flexible randomization and trial supply management (RTSM) systems (sometimes referred to as interactive response technology, or IRT), as they can alter treatments and randomization […]

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Reading Time: 3 minutesEvery step of a clinical trial must be executed effectively and efficiently to maximize the chances of its success. Medidata is introducing “Your Technology Roadmap Through the Clinical Trial Process”, a new, interactive tool to guide early-stage, small, and mid-sized pharma and biotech companies through discovering and assessing their optimal technology path. Read on to […]

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Reading Time: 4 minutesThis blog was authored by the Medidata Patient Insights Board. The best way to stay up to date with key issues facing patient populations in a given disease state is to attend a Food and Drug Administration (FDA) listening session. The Patient Insights team at Medidata regularly attends these sessions to make sure the patient perspective […]

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Reading Time: 2 minutes Lately there’s been questions about the accuracy of mHealth wearable devices.

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Reading Time: 2 minutes If your trials rely on research participants with a track record of taking part in a number of clinical trials, it might be worth taking a second look and examining them a bit closer.

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Reading Time: 2 minutes As with most businesses, a big concern for clinical trial sites is paying the bills. Sites typically receive payments for work performed about four months late while bills are due upfront.

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Reading Time: 2 minutes With the government’s reauthorization of the Prescription Drug User Fee Act in 2012 (PDUFA V), the FDA is trying an experiment to gather patient input by disease group rather than an individual treatment.

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Reading Time: 4 minutes The mHealth landscape is expanding with over 97,000 apps (mobile applications) as of 2013.

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Reading Time: 3 minutes This blog was authored by the Medidata Patient Insights Board. The best way to stay up to date with key issues facing patient populations in a given disease state is to attend a Food and Drug Administration (FDA) listening session. The Patient Insights team at Medidata regularly attends these sessions to make sure the patient […]

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Reading Time: < 1 minutes We recently caught up with James Moon, a biostatistician at the Fred Hutchinson Cancer Research Center.

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Reading Time: 3 minutesClinical trial planning and execution are notoriously difficult, as they require consideration of a number of complex operational, clinical, and social factors. One of the largest hurdles biopharmaceutical companies and CROs face is clinical trial enrollment. As of April 2022, it’s estimated that 11% of clinical research sites fail to enroll a single patient1. Nearly […]

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Reading Time: 3 minutes Wearable devices receive plenty of attention in the consumer setting, and they are now receiving increased consideration in the clinical setting as well.

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