September 20-23, 2010 | Philadelphia, PA

Why Attend

"Very good speakers and subject matter and was filled with information rather than basic concepts."
- Logistics Project Manager, Bilcare Inc.

More Testimonials

What was discussed at the 7th Cold Chain Distribution for Pharmaceuticals

Transportation & Logistics Plenary:

  • KEYNOTE: by Edward Kelly, US Department of Homeland Security on Qualifying for the TSA Cargo Screening Program
  • AIRLINES FOCUS: "Interview with Airlines" and discussions on TSA Cargo Screening & meeting new IATA guidelines – hear from leading airline carriers including American Airlines, Cathay Pacific, Air France KLM, United Airlines, Air Canada, & Delta
  • 'Hot topic' workshop: Quality & Efficeincy for Cost & Temperature Controlled Transportation

Last Mile Logistics

  • Role of the Wholesaler in the Distribution of Temperature-Controlled Products – a presentation by McKesson
  • Distributing Cold Chain Products to the Public & Emergency Planning – a presentation by the Public Health District Leader, Alexandria, Virginia

Biological Materials & Clinical Supplies:

  • Quality Control for the Storage and Transportation of Blood and Biologics - American Red Cross
  • Global Logistics for the Clinical Distribution of Cytotoxic Antibody-Drug Conjugates - Seattle Genetics
  • Cold Chain Planning and Shipping of Bulk Protein Internationally at -60°C – Novartis

Regulatory and Guidance updates from the PDA, MHRA, Health Canada and US Pharmacopeia:

  • Implement new guidance including Revised Technical Report 39
  • IATA Chapter 17
  • USP Revised <1079>
  • FDA Points to Consider
  • European cold chain guidelines and new market regulatory perspectives

Plus – don’t miss hearing from your industry colleagues on Managing International Cold Clinical Supplies, during the NEW Focus Day, including the topics:

  • Clinical cold chain regulatory requirements
  • Validating smaller packaging
  • Factoring in humidity, vibration and variability of loads
  • Tricks to obtaining customs clearances in new markets
  • Controlled Room Temperature (CRT) storage and supply of clinical trial material according to FDA expectations
  • Quality and temperature control downstream at clinical sites

Who should attend?

Vice Presidents, Directors and Managers in the Pharmaceutical industry working within:

  • Logistics
  • Distribution & Transportation
  • Warehousing
  • Packaging
  • Quality Assurance & Quality Control
  • Regulatory Affairs & Compliance
  • GMP
  • Validation

Past Attendes Snapshot of who attended last year
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Audience Profile by Department

Audience Profile by Department