Clinical Research

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19 12, 2018

Key Expectations of Clinical Trial Operations Leaders in 2019

2019-08-02T15:47:54-04:00

Today’s clinical trial operations leaders are in a challenging and expanding role. You are expected to increase study capacity, manage more complex trial protocols, accelerate study startup, and ensure timely sponsor collaboration - all while remaining hamstrung by limited resources, siloed data, stronger regulations, changing sponsor demands, and a growing site footprint. Clinical [...]

Key Expectations of Clinical Trial Operations Leaders in 20192019-08-02T15:47:54-04:00
7 08, 2018

Ten Must-Have Capabilities When Evaluating eRegulatory Platforms

2020-03-03T13:29:55-05:00

Successfully transitioning your team to an eRegulatory solution, while avoiding costly compliance mistakes and realizing true time-saving benefits, requires careful evaluation of potential platforms. After helping thousands of research teams implement eRegulatory, our team has put together these ten essential capabilities to look for when evaluating solutions. You can download our full Guide to Selecting [...]

Ten Must-Have Capabilities When Evaluating eRegulatory Platforms2020-03-03T13:29:55-05:00
25 10, 2017

Roadmap to eRegulatory: Define Eight Critical Workflows

2019-08-02T16:07:36-04:00

Transitioning to an eRegulatory platform is full of benefits; accelerated study startup, centralized document management, the ability to review and sign documents anywhere, easy task management, remote monitoring, and more. After hundreds of successful site implementations, our team has developed a complete guide for clinical research sites and centers planning for eRegulatory, available here. [...]

Roadmap to eRegulatory: Define Eight Critical Workflows2019-08-02T16:07:36-04:00