WEBINAR: Conducting Monitoring Visits Remotely for IVD Clinical Trials During the COVID-19 Pandemic

IVD Sponsors and CROs are tasked with identifying new processes and systems to facilitate clinical trial monitoring and management remotely due to COVID-19 restrictions. This requires developing and implementing plans to continue subject enrollment, sample collection and testing, efficient data collection and monitoring without the benefit of in-person, on-site review. The use of technology and innovation are critical to perform these clinical study tasks remotely and keep projects on track. During this webinar, Beaufort will review a case study that details the required planning and implementation of best practices to conduct monitoring visits remotely, including:

  • Factors in the Sponsor/CRO Assessments/Decision-making processes:
    • Which sites are equipped to participate in monitoring visits performed remotely?
    • Which types of visits can be performed remotely and related key considerations?
    • What technologies & processes can be used to remotely review source documents & site binder documents?
    • How to effectively communicate with the Principal Investigator and site staff without being on site?
  • Required updates to study documentation
  • Risks and Mitigations
  • Application of lessons learned to future clinical trials

Interested in learning more about Beaufort can help your business? Email us at [email protected] or submit your request today.

WATCH WEBINAR

This webinar was recorded on November 3, 2020 in collaboration with Q1 Productions. Beaufort presenters were:

Trish Landry, MBA, RAC, CCRP, Senior Vice President, Clinical Operations

Leah Hollins, MPH, BA, Senior Clinical Project Manager