Webinar On Risk Management and Risk Analysis Techniques in Clinical Trials
September 8, 2014 - Mississauga ON CACompliance Trainings
suzzane.d@compliancetrainings.com
Phone:4169154458
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