This event features two days of interactive workshops, presentations, panels and roundtables, all developed for smaller companies with limited resources.  

Join us to gain a comprehensive education on clinical risk management and the tools to assess, maintain and mitigate risk to ensure compliance.

2019 Audience Demographics

TOP REASONS TO ATTEND

Having successfully established a series of clinical quality events on the East Coast and in Europe, ExL Events brought their well-known conference series to San Francisco in 2019, with a Clinical Trial Risk Management Seminar geared towards biotechnology and biopharmaceutical companies.  With a successful first year under our belts, we are excited to come back and continue to provide the educational needs for smaller companies with limited resources.

  • Understand the value of risk-based approaches to ensure compliance using limited resources.
  • Ensure your clinical quality risk management plan covers all the critical elements to ensure GCP compliance.
  • Develop an effective strategy to work with and oversee your CRO partners to ensure transparency, compliance and productivity.
  • Learn the tools to achieve a constant state of inspection-readiness.

Who Should Attend

This conference is designed for professionals from pharmaceutical, biotechnology and medical device companies; CROs; and other clinical trial service providers whose responsibilities involve the following:

  • Good Clinical Practice (GCP)
  • Clinical Quality Assurance (CQA)
  • Clinical Quality Control (CQC)
  • Clinical Trial Operations/Management
  • Clinical Research
  • Quality Management/ Global Quality Management
  • Audits/Inspections
  • Compliance/Global Compliance
  • Data Management/Systems Operations
  • Clinical Monitoring
  • Regulatory Affairs
  • Safety and Risk Management/Operations

 

The event is also relevant to clinical QA, compliance and operations professionals from:

  • Quality Service Providers and Consulting Companies
  • CROs
  • Central, Imaging and ECG Labs
  • Investigative Sites
  • IRBs
  • Data Management and Software Vendors
  • Safety Reporting Vendors