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JUST ANNOUNCED: The 9th Annual Proactive GCP Compliance Conference, March 2018 in Philly!

Everyone at ExL Events is excited to announce that our 9th Annual Proactive GCP Compliance Conference will take place on March 19–21 at the Sheraton Philadelphia University City Hotel. Now in its ninth year, ExL’s Proactive GCP Compliance conference continues to act as the annual forum for both senior-level clinical quality and clinical operations executives to gather, learn and discuss strategies to achieve and maintain global GCP compliance. Join us to learn how to effectively build quality risk management approaches into your clinical operations to optimize research, maintain GCP compliance, contain costs and ensure patient safety.

Some topics that we are considering for the upcoming conference include:

  • Examining the Global Regulatory Environment and the Impact on GCP
  • Ensuring Data Integrity Across All Stakeholders and Processes
  • Operationalizing Risk-Based Monitoring
  • Achieving a Constant State of Inspection Readiness
  • Implementing an Effective Quality Risk Management System
  • Having an Inspection-Ready Trial Master File
  • Measuring Quality and Tracking Data to Mitigate Risk
  • Developing a Proactive Risk Management Plan
  • Optimizing Education and Training to Ensure Compliance

We are currently shaping the agenda and would love to hear from you!

  • What are the GCP-related topics of most concern?
  • Where are you facing challenges?
  • How would you like to improve your clinical quality and risk management operations?

Get Involved!

Click here to let Senior Event Director, Kristen Hunter, know you’d be open to a brief call to share your thoughts and experiences. You can also discuss the possibility of sharing your expertise as a member of the speaking faculty — if that is of interest to you.

If you are interested in learning more about exhibition and sponsorship opportunities, please contact Justin Kreamer at 917-932-0429 or

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

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