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10 Tips for Submitting Human Subjects Protocols

 
  September 11, 2012  
     
 
ComplianceOnline, Online Event
2012-10-10


Why Should You Attend:

In conducting human subjects research, an investigator must send his/her protocol to the Institutional Review Board (IRB) for approval. Often seen as “black holes” that one submits to and awaits a determination, submitting a study to an IRB can seem like an arduous, daunting task. Because of this, investigators are always looking for tips that will make this process less mysterious and faster.

This session is designed to remove some of the mystery of an IRB submission by providing tips on simple steps that may be taken by the investigator/research team in preparing his/her submission making it more IRB ready and therefore receiving less contingencies which in turn speed up the IRB review and approval process.

Areas Covered in the Seminar:

  • What holds up your study in review?
  • When to submit to an IRB.
  • When is an individual or institution engaged?
  • Regulatory requirements for engagement.
  • What is considered human subjects?
  • When is your activity research?
Event Details:
 
Date:                     October 10, 2012
Time:                     10:00 AM-11:00 AM PDT
Cost:                      $249 per attendee per computer terminal
Registration:          SIgn-Up on-line now.  Add to your shopping cart.
 
 
Organized by: ComplianceOnline
Invited Speakers: Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for human subject research which has served as a model for other institutions. She crafted budgets, policies, procedures, reporting, and training for the new program.
 
Deadline for Abstracts: 2012-10-10
 
Registration: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702475?channel=hummolgen
E-mail: referral@complianceonline.com
 
   
 
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