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