Quality Research Essentials: Best Practices For Quality, Compliant Clinical Trials

In essence, it's quite straightforward: Quality research is an absolute must. The expectations of stakeholders, your financial bottom line, and the well-being of patients all hinge on your ability to conduct a compliant, secure trial that efficiently and safely brings your product to market. However, the realm of regulations, FDA guidance, and other governing factors is undeniably complex. So, how can you effectively navigate these intricacies to ensure every aspect of your trial maintains high quality, stands up to scrutiny, and safeguards patient interests?

Enter "Quality Research Essentials: Don't Become the Next Cautionary Tale," a webinar from the Elligo Elite Learning Series. This open roundtable discussion, featuring industry leaders such as Julieann Blasingim, VP of Compliance and Development at Elligo Health Research®; Debra Fontana, Consultant at Polaris Compliance Consultants, Inc.; and Linda McCarty, Chief Legal Officer and Privacy Officer of Javara, explores various facets of conducting high-quality, compliant clinical trials. It covers crucial topics like FDA inspection trends, risk reduction strategies, common findings from 2022 site and sponsor inspections, approaches for quality assurance and risk management, practical compliance tips, and offers an interactive Q&A session.

Gain insights into how you can ensure all aspects of your trial are high quality, will withstand scrutiny, and protect the patient by accessing the full article below.