Clinical Trials Inspection Readiness Summit

Description

The Clinical Trials Inspection Readiness Summit covers topics such as:

  • The success of your clinical trial using metrics that measure the performance of CROs and trial sites
  • Crucial information and analyze regulations from around the world, with a focus on FDA, EMA, PMDA and MHRA regulations
  • Process maps that can be applied to streamline TMF management and the key team members who need to be involved
  • Strategies for ensuring there is a comprehensive clinical trial storyboard so inspectors can recreate the trial

The Clinical Trials Inspection Readiness Summit brings together:

  • Clinical Operations
  • Quality Assurance/Quality Control/Quality Compliance/Quality Management
  • Clinical Trials Management
  • Records/Data Management
  • TMF/eTMF
  • Global Compliance
  • Clinical Research
  • Clinical Monitoring
  • Auditing
  • Safety and Risk Management/Operations
  • Trial Master Files
  • Clinical Project Management
  • Clinical Document Coordination
  • Clinical Development
  • Global Regulatory Affairs
  • Clinical Site Management

Future Events

Past Events

Important

Please, check the official event website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Quality assurance, Security & Safety
Health & Medicine: Medical device, Medical laboratories, Medical technology, Pharma

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