The criteria covered in 21 CFR Part 11 are not the only requirements that should be considered for compliant document management associated with clinical trials.
Use these best practices to effectively build and implement eCRFs for your clinical trials and see higher quality data collection at your research organization.
We created a way to help cancer centers demonstrate collaboration for CCSG application and renewal. Product Manager, Jeremy Shapiro, explains our process for finding a solution.
Forte’s Founder & CEO, Shree Kalluri, shares his vision for the future of information exchange in clinical research.
Expert webinar presenter answers attendee questions about what to expect from your research system point of contact, when and how to mandate system training, and how to increase the value you see from your research systems.
At the 2018 Fall Onsemble conference, we introduced a wide array of product and services enhancements to help customers take their research operations to the next level.
Watch this on-demand webinar to hear Director of Analytics, Wendy Tate, discuss the top three practices identified by survey respondents as critical to the success of research systems at their organization.
Like all Onsemble Conferences, this week was an opportunity to make meaningful connections with peers from top research institutions and work together to find powerful solutions for the research industry’s most pressing challenges.
Leading research organizations discuss the clinical research industry’s most pressing challenges and generate powerful ideas for clinical trial efficiencies at the 2018 Fall Onsemble Conference.