6th Signal Detection, Root Cause Analysis & CAPA Summit - Arlington, VA

6th Signal Detection, Root Cause Analysis & CAPA Summit
January 21 - 22, 2016
Arlington, VA
Arlington, VA

Prevent Non-Compliance and Achieve Successful Root Cause Analyses and CAPA System Implementation from Clinical to Post-Market

6th Signal Detection, Root Cause Analysis & CAPA Summit – 6th Signal Detection, Root Cause Analysis & CAPA Summit

Weather Update: The 6th Signal Detection, Root Cause Analysis & CAPA Summit is still on as scheduled. We are keeping a close eye on the weather report to see if any schedule changes need to be made to our agenda to accommodate our guests.

As the only forum dedicated to identifying clinical and postmarket non-compliance, understanding the root cause, and responding with appropriate corrective and preventive actions, the 6th Signal Detection, Root Cause Analysis & CAPA Summit has become the annual gathering for life science professionals in the areas of quality, compliance, regulatory affairs and risk management from companies of all sizes and types to discuss and share their experiences.

Now in its sixth year, this conference will address the main considerations for implementing a full and efficient CAPA system in the premarket and postmarket arenas, while ensuring quality and supporting product safety and compliance. Join us in January to receive unmatched detail on how to construct root cause analysis methodologies and remain in compliance from clinical to postmarket stages!


Featured Speakers Include:


Top Five Reasons to Attend

  1. Learn about tools, challenges and considerations for the implementation, verification and validation of CAPAs
  2. Address ways to prepare for inspections and determine a course of action when dealing with inspection findings
  3. Discuss root cause analysis and CAPA implementation in big vs. small companies
  4. Hear about proactive risk management to prevent the cause of nonconformities in pharmaceutical and medical device companies
  5. Explore vendor and technology management in the CAPA landscape, and ways to address systemic vs. non-systemic issues

Who Should Attend

Pharmaceutical, biotech and medical device professionals responsible for:

  • Quality Assurance/Quality Control/Quality Compliance
  • R&D Compliance
  • GCP Compliance
  • Clinical Auditing
  • Quality Systems/Processes
  • Regulatory Affairs
  • Clinical Development/Operations
  • Quality Training
  • Data Management/Data Analysis
  • Clinical Monitoring
  • Post-Market Compliance
  • Validation
  • CMC
  • Pharmacovigilance Quality Assurance
  • Continuous Improvement

This Event May Also Be of Interest to:

  • Compliance/Quality Assurance/GCP Consultants
  • Data Management and Quality Systems Management
  • CAPA Systems Management
  • Audit Tracking and Management
  • Trial Master File Professionals
  • Metrics Professionals
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