Sponsor Management of Investigator Non-Compliance

Oct 6, 2018, 18:21 PM
Course ID : 067
Acronym : INC
Get Barnett International's expert guidance to manage investigator non-compliance. Act now for success!

Course Description

Investigator non-compliance to the Statement of Investigator commitments has increased in many areas. One of the identified causes has been monitoring. Investigator compliance issues are great risks to product development success, but an even greater risk to sponsors is the lack of formal systems to manage compliance at research sites.

With the promise of more sponsor inspections, the sponsor management of investigator non-compliance is an obligation that requires comprehensive management approaches that lead to control of investigational product, data integrity, and adequate documentation for regulatory inspection of sponsors monitoring programs and/or investigative sites. Seven steps in compliance management of research sites will be presented for the participants to assess their current practices for gaps and risks for preparing for potential regulatory inspection evaluating compliance management of research sites.

Learning Objectives

  • Categorize investigator non-compliance
  • Define adequate escalation of non-compliance
  • Summarize proactive investigator training related to sponsor’s response to non-compliance
  • Employ seven comprehensive steps in compliance management
  • Detect trending to better anticipate compliance issues

Who Should Attend

  • Sponsor Senior Management
  • Project Managers
  • Clinical Research Associate Managers
  • Clinical Research Associates
  • Quality Assurance/Compliance Personnel

Instructor

Janet Ellen Holwell, C.C.R.C., C.C.R.A., T.I.A.C.R., F.A.C.R.P.

Click here for complete trainer biographies

Registration Fees

$735

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: customer.service@barnettinternational.com 

Accreditation Information

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#: 0778-0000-22-010-L04-P. Released: 2/22. 

Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.  

Series :
  • Clinical Trials & Translational Medicine
Topics :
  • Clinical Research
Job Functions :
  • Clinical Operations & Trial Management
  • Clinical Quality Assurance
  • Clinical Research Associate
  • Project Manager
  • Regulatory Affairs
  • Study Site Compliance
  • Training
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