While the Common Rule is critical to ensuring the ethical conduct of human subjects research, it can be difficult to navigate the changing requirements. We’ve compiled some helpful resources to assist in getting to know the Common Rule.
Learn how a CTMS can help you beat these common struggles and increase productivity at your clinical research site.
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.
As natural and man-made disasters have become more prevalent in the healthcare industry, it’s important for research organizations to ensure they have well-defined business continuity and disaster recovery plans.