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    Webinar On Risk Management and Risk Analysis Techniques in Clinical Trials

    View: 228

    Website https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1310 | Want to Edit it Edit Freely

    Category Food, Drugs & Biologics, Risk Management, Risk Analysis Techniques, Clinical Trials, risk factors in clinical trials, clinical trial operations, medical product development, clinical trial management, clinical trial development, biological sample handling, regulatory trouble shooting, clinical trial development

    Deadline: September 08, 2014 | Date: September 08, 2014

    Venue/Country: Mississauga, Canada

    Updated: 2014-08-25 18:30:05 (GMT+9)

    Call For Papers - CFP

    This seminar will provide the basics of clinical trial risk management and analysis techniques and practical tips to clinical trial professionals and sponsors using case studies from the presenter’s experiences.

    Areas Covered in the Session :

    Common risk factors in clinical trials

    Retrospective and prospective risk analysis techniques

    Risk management: Key techniques in risk reduction, assessment, addressing, training and communication

    Risk analysis plan: identification, information gathering, decision, implementation and review

    Roles and responsibilities of various personnel in risk reduction

    Overview of FDA requirements for risk management

    Expectations and responsibilities of the clinical project manager

    Role of various clinical team members: CRA, coordinators, sponsors and investigators

    Challenges of large-scale and international clinical trials

    Do’s and Don’ts for risk management of a clinical trial

    Who Will Benefit:

    Clinical Project Managers

    Clinical research associates

    Clinical coordinators

    Principal Investigators and sub investigators

    IRB personnel

    Regulatory Vice Presidents, Directors and Managers at sponsors

    Attorneys ? In-house or Outside Counsel

    Price tags:

    Live

    Single Live : For One Participant

    $ 249

    Corporate Live : For Max. 10 Participants

    $ 899

    Recording

    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 : supportatcompliancetrainings.com


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.