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POST ID: 5504

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

Region: Canada
Location: 5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Cana


This 1 hour virtual seminar will help you understand the key issues and challenges associated with investigator initiated trials. Investigator initiated trials are very important as they are important connection for the translation of research from bench to bedside. I will discuss the role of sponsor-investigator and ways we can ensure the protection of human subjects in an investigator initiated trials.
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. Despite availability of an ample amount of resources that are available for some studies, but are lacking in the studies that are innovatory, collective or questionable. To ensure protection of human subjects in clinical trials participation how sponsors, investigators and site can ensure vigilance in this process.
Areas Covered in the Session :
This webinar will introduce the learners regarding main areas of investigator initiated trials and the necessary steps taken to ensure compliance with federal regulations and the International Conference on Harmonization. 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
Recognize the resources available to help the investigator in the conduct of investigator-initiated trials
Who Will Benefit:
This topic applies to personnel / companies doing research or involved in the clinical trials. The following will benefit:
Principle Investigators(PIs)
Senior Clinical Research Associates(CRAs)
Clinical Research Project Manager
Contract Research Organizations (CROs)
Clinical Research Coordinators
Institutional Review Boards (IRBs)
Site Management Organizations (SMOs)
Price tags:
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299

For more information Contact
Compliance Trainings
5939 Candlebrook Ct,
Mississauga, ON L5V 2V5, Canada
Customer Support : 416-915-4458
Email :

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