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The nature of managing clinical research has evolved greatly since the initial clinical trial management systems (CTMS) and other early eClinical technologies were introduced. As the traditional trial paradigm has shifted, new technologies have been introduced and existing ones have evolved to keep up with the industry.

There’s no denying that the medical device industry has seen a tidal wave of competition in recent years. Forbes forecasted that this $518 billion industry will be a disruptor in the healthcare technology space through 2023, if not longer.

This webinar session focused on how Medrio’s integrated RTSM solution can be optimized to reduce the noise of complicated clinical trials and leave you with clear, actionable data for better supply management.

This webinar session focused on how Medrio’s RTSM solution can be optimized to reduce the noise of complicated clinical trials and leave you with clear, actionable data for better supply management.

Part 1 of our series looked at how eConsent strengthens your consent process to ensure better patient comprehension, adherence, and retention. Our experts Melissa and David are back to dig into ePRO and how you can set your study up to achieve as much as 97% compliance with patient reported outcomes.

It’s no secret that patient recruitment and retention is one of the most significant challenges in clinical studies. With 35% of patients who dropped out of trials citing the consent form as confusing, you have an opportunity to ensure that your study’s consent process is simplified and designed for patient comprehension.