Ensuring Compliance, Quality & Efficiency in Your Clinical Trials Supply Chain

As you may know, the FDA has confirmed that as part of its Critical Path Initiative “Streamlining Clinical Trials” is one if its key priorities. Implementing a new operating model that supports integrated processes, inventory visibility, and compliance in manufacturing and distribution of clinical trials are key to the growth of pharmaceutical and biotechnology companies because of its major contribution to the overall cost of drug development. Clinical trials, being an essential part of the product development process, if run efficiently can provide the company with a competitive advantage.

The 3rd Annual Clinical Trials Supply & Logistics Summit, previously known as the Clinical Trials Logistics Summit, will give you expert knowledge and experience to prepare you with the skills and tools needed to use clinical trials to gain a competitive edge in the pharmaceutical and biotechnology industries.

For insight into summit topics, read Improving Clinical Data Management Through CDISC Standardisation: Clinical trials are taking place on an increasingly global scale and are under rising pressure as companies look for the fastest and most cost effective way to get their product to market.

Data standardization is one way through which firms can help achieve these aims.

The expanded 3rd Clinical Trials Supply & Logistics Summit will address:

  • Domestic and international regulation and guideline variations
  • Light timelines and limited supplies
  • Emerging markets: regulations & logistics
  • Right drug, right place, right time at the lowest price
  • Stakeholder alignment
  • Accurately forecasting clinical trial supply demands to reduce costs
  • Staffing and training throughout the clinical trial supply chain process
  • Clinical Trial Productivity Metrics & ROI

In addition to hearing case studies on special cases: biologics, temperature control, and adaptive trials, you will be able to select your track from Planning/Procurement or Manufacturing and Distribution.

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Click here for a preview of session topics.

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Case Studies & Best Practices from These Leading Industry Experts:

  • Rafik H. Bishara, PhD
    Technical Advisor
  • Steve A. Jacobs, MBA, R.Ph.
    President
    Global BioPharm Solutions, LLC
  • Gary Hutchinson
    President
    Modality Solutions LLC
  • Ray Goff
    Former Director
    Pfizer Vaccines R&D
  • David Burnell
    Assistant Branch Chief
    TSNM/CCSP, US
  • Alain Frix
    Clinical Trial Materials Consultant
    Chorus, Eli Lilly
  • Dr. Anoop CH.
    Clinical Research Physician
    Stempeutics Research Pvt. Ltd

View snapshot of speakers

Those attending the 3rd Annual Clinical Supply Chain include:

VP’s, Directors, Heads, Managers of:

  • Clinical Trial Supply
  • Clinical Trial Operations
  • Clinical Trial Logistics
  • Investigation
  • Project Management
  • Research and Development
  • Packaging
  • Distribution
  • Materials
  • Clinical Trial Purchasing
  • Outsourcing
  • External Alliances
  • Clinical Research
  • Clinical Trials & Customer Services
  • R&D
  • Quality Control/Assurance
  • Clinical Safety
  • Scientific Affairs
 

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