6th Clinical Quality Oversight Forum -

6th Clinical Quality Oversight Forum
October 5 - 7, 2015
Philadelphia, PA

Ensuring Trial Integrity by Effectively Assessing, Optimizing and Managing the Quality of Clinical Vendors and Sites

6th Clinical Quality Oversight Forum – 6th Clinical Quality Oversight Forum

ExL’s 6th Clinical Quality Oversight Forum, taking place October 5-7 at the Sonesta Hotel in Philadelphia, focuses on ensuring trial integrity by effectively assessing, optimizing and managing the quality of clinical vendors and sites. This forum acts as the annual gathering for clinical quality, operations, management and audit professionals to engage and candidly share their experiences, struggles, obstacles and achievements when working with varying clinical partners, including CROs and investigator sites. Learn from this experienced group and take away proven, results-driven, risk-based strategies for optimizing your company’s clinical vendor and site oversight approach.

Featured Sessions

featured Speakers

Top Five Reasons To Attend

  1. Learn from the industry’s leading clinical operations and quality experts as they candidly share their experiences, strategies and guidance for selecting and managing your clinical partners to ensure compliance and maximum performance.
  2. Benchmark your clinical quality oversight strategy against other similar-sized companies to ensure your approach is optimal and effective.
  3. Integrate risk-based approaches for effectively selecting, monitoring and managing your clinical vendors and sites — while optimizing your resources.
  4. Position your trial for success by ensuring your clinical vendors and sites are inspection ready with the latest tools, technologies and audit strategies.
  5. Design your own agenda and choose your preferred learning environment with the selection of interactive workshops, session tracks, educational presentations, dynamic panels, interactive roundtables and ample networking opportunities.

2014 Audience Profile

Who Should Attend

Professionals from pharma, biotech and medical device companies; CROs; and other clinical trial service providers whose responsibilities involve the following:

  • Quality Management/Clinical Quality Management
    • Clinical Quality Assurance/QA/CQA
    • Clinical Quality Control/QC/CQC
  • Clinical Operations/Management/Research/Development
  • Compliance/Clinical Compliance/Regulatory Compliance
  • Monitoring/Site Management/Study Management
  • Clinical Outsourcing/Vendor Management/Third Party Management
  • Good Clinical Practice/GCP
  • Auditing
  • Clinical Risk/Risk Assessment
  • Regulatory Affairs
  • Medical Affairs

This event is also of interest to:

  • Investigative Sites
  • Academic Research Organizations
  • Central, Imaging and ECG Labs
  • IVRS Companies
  • EDC Companies
  • Other Clinical Service Providers
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