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Webinar On Risk Management and Risk-Based Monitoring

This course provides an understanding of risk management principles and makes the links between study level risk management and the implementation of risk based monitoring.

On Going Christmas Offers: Offer valid till 1 st January 20151. Register an attendee for Single Live:Get 10% of on every RegistrationFirst 10 attendees will receive recording Access to the webinar for No Additional CostFor Coupon Code call customer support:  416-915-44582. Register your Group for Corporate Live:Get 15% of on every RegistrationEvery group registrant will receive Recording Access to the webinar for No Additional CostFor Coupon Code call customer support: 416-915-44583. Unlimited viewing for 4 days4. The discounted amount will appear after entering the Coupon Code in the Secure Check out PageThis course provides an understanding of risk management principles and makes the links between study level risk management and the implementation of risk based monitoring.New regulations with regard to Risk Based Monitoring were released by FDA in August 2013 to build on those for Quality Risk Management (ICH Q9) released in 2005 by ICH and 2006 by FDA. In addition there is permanent pressure on resources for clinical trials and it is vital that those precious resources are utilized there they deliver greatest benefit.The implementation of risk-based study specific monitoring strategies, plans will be a critical component for every study sponsor to ensure high quality and integrity of data, enhance human subject protection, reduce cost and eliminate inefficiencies across clinical trial process. Thorough identification and evaluation of risks to critical study data, processes and thereby designing appropriate monitoring plan with a balance of centralized & onsite monitoring will maximize the effectiveness of risk based monitoring.Considering the importance and need of risk-based monitoring currently in clinical trial management, it is recommended to attend this webinar that provides more insight on this new approach.Areas Covered in the Session :Regulatory requirementBroad review of risk based activitiesStudy level risk managementRBM – adding value to your operationsWhat may generate risk?Risk management documentation/risk statement structureHow to get startedActions and how to manage themPractical implicationsWho Will Benefit:A must attend webinar for allClinical Research AssociatesMonitorsData Management TeamProject Management StatisticiansClinical Research OutsourcingDrug SuppliersAll clinical research professional embarking on a risk-based approachPrice Tags:LiveSingle Live : For One Participant$ 249Corporate Live : For Max. 10 Participants$ 899RecordingSingle REC : For One Participant - Unlimited Access for 6 Months$ 299For more information and enquiries contact us atCompliance Trainings5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada  Customer Support : #416-915-4458

When

2 Feb 2015 @ 01:00 pm

2 Feb 2015 @ 02:00 pm

Duration: 1 hours

Timezone: GMT -5:00


Where

Online Webinar


Organised by

Compliance Trainings (deactivated)

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