Investigator initiated trials- What are we doing to ensure human subject protection?

Duration: 60 Minutes
Investigators initiated trials are very essential of any research to be translated from bed to bedside. The inception of these research are only done with a scientific interest in a new or existing drug or device, generate new ideas, and mostly involve collaborative research between different departments and also different types of researchers.
Investigator Initiated Trials
Instructor: Dr. Nagina Parmar
Product ID: 500222
Despite availability of an ample amount of resources that are available for some studies; however are lacking in the studies that are innovatory, collective or questionable. To ensure protection of human subjects in clinical trials participation sponsors, investigators and site can ensure vigilance in this process by exploring the resources and tools that are available to the researchers.

Why Should you Attend:
This topic applies to personnel / companies /academic institutions doing research or involved in the clinical trials.

Objectives of the Presentation:
Upon completion of this webinar, attendees should be able to:
  • Recognize the importance of investigator-initiated trials
  • Identify way to ensure human subject protections
  • Identify the investigator deficiencies
  • Identify what are the site responsibilities in investigator initiated trials
  • Identify the approaches or concerns of Institutional Review boards
  • Recognise the resources available to help the investigator in the conduct of investigator-initiated trials.
Who can Benefit:
This topic applies to personnel / companies doing research or involved in the clinical trials. The following will benefit most include:
  • Principle Investigators
  • Senior Clinical Research Associates(CRAs)
  • Clinical Research Project Manager
  • Contract Research Organizations (CROs)
  • Institutional Review Boards (IRBs)
  • Site Management Organizations (SMOs)
$300
Recorded Session for one participant
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  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
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  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Dr. Nagina Parmar has 15 years of clinical research experience as a certified clinicalresearch professional in academia and hospital. Her expertise as clinical research professional lies incoordinating various Phase I, II and III national and international clinical trials and investigator initiatedtrials. During 15 years of career as CCRP, she was also involved in developing SOPs (Standard operatingProcedures), REB SOPs and research elements database. She is an active member of the Society ofClinical Research Associates (SoCRA) and Network of Networks(N2N).

As an Adjunct faculty, Dr. Parmar isalso involved in teaching Biology, Microbiology, Life Sciences for Clinical practice, and drug developmentcourses at various academic institutions. Her writing appeared in more than 30 journal articles, booksand reviews in various national and international journals. As a mentor, Dr. Parmar provides guidanceand career counseling to assist students with their endeavors. Dr. Parmar has given various careerdevelopment seminars at University of Toronto to graduates and postgraduates and webinar withAssociation of Clinical Research Professionals (ACRP).
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