The FDA’s Guideline for the Monitoring of Clinical Investigations (1988-2010) has been removed from the FDA list of guidance documents. Instead, the FDA has released an updated version of the Bioresearch Monitoring (BIMO) Compliance Program Guidance Manual for Sponsor/CRO and Monitoring, and most recently the agency released a draft guidance to reflect their expectations and recommendations related to monitoring investigation sites, monitoring systems, and investigative site oversight. In this web seminar, the content and the implications to sponsor monitoring and clinical investigation sites will be discussed.
- Explain ways in which the regulatory climate is reflected in the new monitoring guideline
- Discuss the content of the guideline in relation to traditional monitoring plans
- Assess the implications of the guideline to current monitoring practices and relationships with oversight of Clinical Investigator
- Clinical Research Associates
- Study and CRA Managers
- Clinical Investigators and Staff
- Sponsors/CROs Clinical Operations
- Clinical Quality Compliance and Quality Assurance Professionals
Sandra “SAM” Sather, M.S., B.S.N., C.C.R.A., C.C.R.C.
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$695
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 1-800-856-2556 for pricing.
Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 1.5 hours (0.15 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will mail ACPE statements within three weeks of program completion. ACPE#: 0778-0000-11-081-L01-P. Released: 8/11.
Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471.