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Assessing Risk in Human Research Protocols

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					                                                                                           For Assistance
                                                                                           Email: support@mentorhealth.com
 
                                                                                           Phone: 800-447-9407 or
                                                                                           Fax your PO to: 302-288-6884

    Live Webinar           on
 
      Assessing Risk in Human Research Protocols

    Date & Time:                                                                                                                       

     Tuesday, January 29, 2013           10:00 AM PST | 01:00 PM EST
                                                                                                 Register Now                          
     Duration: 60 Minutes                Instructor: Sarah Fowler-Dixon

     Location: Online                    Price : $195.00   (for one participant)

                                                                                            Instructor Profile:
                                                                                                       Sarah Fowler-Dixon
     Overview:                                                                                        Education Specialist and
    45 CFR 46.111 (a)(2) states, "In evaluating risks and benefits, the IRB                           instructor , Washington
    should consider only those risks and benefits that may result from the                                   University

    research (as distinguished from risks and benefits of therapies subjects                Sarah Fowler-Dixon, PhD, CIP is
    would receive even if not participating in the research)." How the study                Education Specialist and instructor
                                                                                            with Washington University School of
    is designed can minimize potential risks to participants. Studies that are
                                                                                            Medicine. She has developed a
    deemed "minimal risk" have greater options when it comes to using an
                                                                                            comprehensive education program
    expedited review system and options for consent.                                        for human subject research which
                                                                                            has served as a model for other
    Risk rating also affects how elaborate a data safety monitoring plan will               institutions. She crafted budgets,
    be required and measures put in place to protect privacy for the                        policies, procedures, reporting, and
    individuals and confidentiality of the data.                                            training for the new program. She
                                                                                            has initiated the planning,
                                                                                            development, authorship and
     Why should you                                                                         implementation of many human
     attend:                                                                                subjects research policies, practices,
                                                                                            guidelines, submission and reviewer
    All researchers want their studies be reviewed and approved quickly.
                                                                                            forms often working with state and
    Risks in the study can slow the process as the level of risk assigned a
                                                                                            federal authorities. ....more
    research protocol affects: mode of review, whether or not additional
                                                                                    
    approvals outside of the IRB are needed,

                                                                                           Suggest a Topic       More Webinars
     Areas Covered in the Session:
                                                                                             Your Necessity is our Priority


        l   What is risk assessment?
        l   Why is risk assessment important?
        l   How can you make preliminary risk assessments?
        l   What does risk assessment affect?                                                                 
        l   What are some methods of reducing risks in a research study?
        l   Examples


    Click here to register for this webinar


     Who Will Benefit:


        l   Principal Investigators / Sub-investigators.
        l   Clinical Research Scientists (PKs, Biostatisticians,)
        l   Safety Nurses
        l   Clinical Research Associates (CRAs) and Coordinators (CRCs)
        l   Recruiting staff
        l   QA / QC auditors and staff
        l   Clinical Research Data managers
        l   Human Research Protection professionals


It would be really nice if you can circulate this mail to all your deserving colleagues who can immensely
benefit from this program.

For more information, please contact the event coordinator. We look forward to seeing you at the webinar.

Best regards,
Event-coordinator
MentorHealth

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