Monitoring Visit Reports for Medical Device Studies
In this web seminar, we will discuss how to write effective monitoring visit reports for medical device studies. Participants will learn the purpose for monitoring investigational sites and the importance of documenting the visit. We will examine the requirements for the documentation in the Code of Federal Regulations and ICH, and discuss how the report is used by various stakeholders. Tools will be provided to enable learners to scrutinize various sections of the report to better document what was accomplished on the visit. This documentation supports the adequate monitoring obligation expected by regulatory authorities.
- Describe the requirements of documenting monitoring activities for a device study
- Recognize the importance of a well written monitoring visit report, auditable by the regulatory authorities
- Manage site and sponsor activities and document them appropriately
Who Should Attend
- Clinical Research Associates
- Contract Clinical Research Associates
- Lead Clinical Research Associates
- Clinical Research Managers
- All other personnel responsible for writing or reviewing monitoring visit reports for device studies
Shana Zink, B.S.
Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556 for pricing.
Note: Due to COVID-19, we understand that most teams cannot currently dial-in together. As such, we are able to offer additional logins at a highly reduced rate. Please contact Barnett Customer Service at +1 781.972.5400 or toll-free in the U.S. 800.856.2556 to register with your additional participants requiring login credentials. Or email Customer Service at: email@example.com
Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 2 hours (0.2 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion. ACPE#: 0778-0000-20-046-L01-P. Released: 7/20.
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.