2009 Speakers

  • Aileen Suliveras
    Director, Cargo Verification, Customs and Border Protection
    Department of Homeland Security
  • Alfred Mottram
    Associate Director, Drug Supply and Materials Management
    Medarex
  • Dawn Furey
    Associate Director, Research Operations
    Merck & Co.
  • Denise I. Webber
    President & Founder, Clinical and Regulatory Operations
    D.I.Webber Consulting, LLC
  • Dick Winokur
    Vice President, Clinical Supply Chain
    Sanofi-Aventis
  • Domenic Veneziano
    Director, Import Operations & Policy
    FDA

Maximizing Efficiency, Safety and Regulatory Compliance Within your Clinical Supply Chain

In today’s drug development climate, clinical supply professionals face a unique set of challenges. These include adhering & complying with stringent regulations, using specialized temperature packaging and monitoring devices, evaluating cost-effective & validated distribution processes, shipping to and from research labs or hospitals and many more.

The Clinical Logistics Supply conference will provide a unique opportunity to optimize logistics, overcome inefficiencies, develop safe vendor relationships and comply with US and international standards for your clinical supply chain.

IQPC’s Clinical Trials Logistics conference will address key areas, including:

  • Overcoming key inefficiencies in your supply chain
  • Understand how and why global supplies effect enrolment
  • Develop successful & safe vendor relationships
  • Comply with US customers for importing clinical supplies
  • Build an effective risk management strategy into your clinical logistics
  • Avoid common mistakes for logistics in emerging countries
  • Address storage and transportation challenges for your clinical trial supplies

Don’t miss the Clinical Data Management Master Class!

Includes case studies on:

  • The effective use of IVRS in clinical trial management
  • Transforming your supply chain to accommodate adaptive trials
  • Data management associated with distribution of temperature-sensitive clinical materials
  • Optimization of capacity planning, resource allocation and scheduling for portfolios of clinical trials

Who should attend?

  • Clinical Supply Operations
  • Clinical Trials Logistics
  • Clinical/Investigational Supplies
  • Shipping and Distribution
  • Clinical Labeling / Packaging
  • Clinical Trials Material Management
  • Clinical Supplies Manufacturing
  • Clinical Quality Assurance/Quality Control
  • Clinical Data Management
  • Regulatory Affairs
  • Import-Export Trade Compliance
  • Project Management
  • Clinical Research / Planning
  • Drug Supply Management

Speakers include:

  • the Food & Drug Administration (FDA)
  • Department of Homeland Security
  • Sanofi-Aventis
  • Pfizer
  • AstraZeneca
  • Merck
  • GlaxoSmithKline
  • Genzyme
  • Takeda
  • Human Genome Sciences
  • Schering Plough
  • Celgene and Gilead Sciences

Download a snapshot of our past attendees

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