Going through an audit at any clinical research site can be a stressful process. Join us for this educational webinar as Chad Adams, Associate Director at the University of Arizona shares the top 10 mistakes made when conducting clinical research, based on top FDA audit findings.
The 2019 PRIM&R AER Conference provided insights into the changing regulatory world, and reaffirmed the importance of technology as processes and regulations continue to evolve.
At any research site, audits are inevitable. Check out these tips and tricks to help prepare your site for your next audit.
Effective budget negotiation is consistently a hot topic for clinical research sites. Here are a few tips to make sure your site gets the most from your negotiations.
Wendy Tate, Director of Analytics at Forte, discusses adding a protocol feasibility committee to improve trial compliance and ethics through proper resource allocation and ensuring that the objectives can be met through proper accrual.
Many sites understand the benefits of moving from paper regulatory binders to an electronic system. But it’s also important to ensure your organization is implementing a system that will fit your regulatory workflows and set you up for long-term success.
Protocol Feasibilities are designed to help clinical research staff determine the possibility of conducting a study. Here’s how to seamlessly work an assessment in before accepting your next clinical trial.