Risk Based Approaches for Clinical Trials 2019

Topics

• Review a risk based approach to protocol design
• Key risk based process/tools and techniques
• Best practice of these new risk requirements
• Understand risk based approach to monitoring/data handling

Who should Attend

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