Forte and ACRP partnered to conduct a survey analyzing the factors that contribute to technology competency and how sites, technology providers and clinical research professionals can work to improve these competencies across the industry.
Integrated research systems can help streamline your operations, centralize workflows and reduce effort across your teams. But choosing your technology providers can have a big impact on long-term success at your organization.
In this webinar, Stuart Cotter, Forte’s Director of Product Success and former Forte eReg Product Manager, and MaryAnn Kempker, Forte’s Computer System Validation Project Manager, provide insight into how your site can proactively plan for audits and monitoring visits.
Having a team of coverage analysts to ensure compliant clinical trial financial management can be invaluable. Learn what to look for in your coverage analysts and how to build a successful team.
The Trial Data Exchange will build a two-sided network, allowing sites and sponsors can easily access and share standardized clinical research data, including critical regulatory documents.
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.
Our expert webinar presenter answers attendee questions about internal communication plans for effective CCSG management, changes to the how the NCI views cancer centers, and more.
Whether using paper, shared drive or vendor-provided systems to manage regulatory documents, research organizations need to ensure their data is safe in the event of a natural disaster.
Expert webinar presenters answer attendee questions about 21 CFR Part 11 compliance and the validation process for electronic systems.
Watch this webinar to hear our expert presenters provide an overview of 21 CFR Part 11 and discuss the roles both organizations and vendors play during the validation process.