Risk Management in Clinical Trials 2018

  • 12 Feb 2018
  • Webinar

Description

Risk Management in Clinical Trials 2018 is a webinar that covers topics such as:

  • Regulations and guidelines which cover risk management applied to clinical study-level risk management
  • New requirements for risk management in clinical trials
  • Key risk based process/tools and techniques
  • The elements of QM system are and what a regulatory inspector would expect to be in place for clinical trials
  • Risk based approach to monitoring / data handling
  • Risk based approach to protocol design
  • Best practice of these new risk requirements
  • Risk based approaches to QC / QA (Auditing)

Risk Management in Clinical Trials 2018 is intended for:

  • Clinical Research Associates
  • Clinical Development Managers and Personnel
  • Quality Assurance Managers and Auditors
  • Clinical Research Archiving and Document Management Personnel
  • Consultants
  • Clinical Development Managers and Personnel
  • Pharmacovigilance /Drug Safety
  • Regulatory Affairs Specialists
  • Study Site Personnel

Past Events

Important

Please, check "Risk Management in Clinical Trials" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Risk Management
Health & Medicine: Medical device, Pharma

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