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Webinar On Risk Management and Risk Analysis Techniques in Clinical Trials

7/16/2014 1:00 PM - 2:30 PM

. 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:


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,


Customer Support : 416-915-4458

Email :

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