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

The increasing complexity and globalization of clinical trials has changed the pre-market environment, with more companies outsourcing operations and investigating emerging markets. This leads to many questions of regulation, and with high costs and strict handling requirements for many biopharmaceutical products entering clinical development, the logistics of clinical trial supplies are more critical than ever.

The 4th Annual Clinical Trials Supply & Logistics Summit will be investigating compliance, quality control, efficiency and logistics in the clinical trials supply chain. This summit promises to provide industry expert insight into best practices, as well as prepare you with skills and tools needed to use clinical trials to gain a competitive edge in this highly competitive global market.

Read this Q&A interview with Advisory Board member Modality Solutions:
“Integrating Your Stability Data Into Your Transport Validation Approach”


Prefer to listen? Access the PodCast here: Integrating Your Stability Data Into Your Transport Validation Approach.
This information will help you outline a transport validation master plan to ensure high quality drug product is available at the clinical trial site.

The expanded 4th Clinical Trials Supply & Logistics Summit will investigate:

  • International regulation and guideline variations
  • Globalization of distribution operations
  • Project management
  • Planning and forecasting supply demands to reduce costs
  • Emerging markets for clinical trials
  • Monitoring and quality control
  • Outsourcing and partnerships

In addition to hearing case studies on clinical trials in emerging markets, specialty biologic shipping, outsourcing logistical operations and project management, this conference will include expert lead panel discussion to conclude both days.

Testimonials

"Great to hear about a standard before it is in place."
– Sr. Clinical Supply Specialist, MEDIMMUNE
"Good level of detail and interactive."
– Global Logistics, ELI LILLY
"Very knowledgeable speakers. Very relevant for distribution."
-Director, Distribution Operations PFIZER

Summit Advisory Board:

  • Rafik Rafik Bishara, PhD
    Technical Advisor
  • Barret-Katz Barrett Katz, MD, MBA
    Executive Director Office of Clinical Trials
    ALBERT EINSTEIN SCHOOL OF MEDICINE
  • Alisa-Wright Alisa Wright
    CEO
    BIOCONVERGENCE, LLC
  • Shelley-Callahan Shelley Callahan, MBA, BBA
    Sr. Director of Marketing
    CRYOPORT, INC.
  • SteveSteven Jacobs, MBA, R.Ph.
    President
    GLOBAL BIOPHARM SOLUTIONS
  • Paul Harber, MS
    Principal
    MODALITY SOLUTIONS

Distinguished Speakers Include:

  • Charles Borromeo Charles Borromeo
    Hazardous Materials Specialist
    UNIVERSITY OF CALIFORNIA
  • Adam Larrabee
    Director of Business Development
    ROCHESTER CLINICAL RESEARCH, INC.
  • Mary Foster
    Chair Expert Committee, Packaging, Storage and Distribution of Drug Products
    UNITED STATES PHARMACOPEIA
  • Rivka Ravid, PhD
    Sr. Scientist
    NETHERLANDS INSTITUTE FOR NEUROSCIENCES
  • Jack Whitley
    Transportation Specialist
    at the US DEPARTMENT OF TRANSPORTATION
  • Angela Britton MS
    Director of Clinical Operations
    FREDERICK NATIONAL LABORATORY FOR CANCER RESEARCH, NATIONAL INSTITUTES OF HEALTH
  • Buzz Hillman Manager
    Trial Supply Management
    JOHNSON & JOHNSON

And Many More!!!

Who will be attending:

SVPs, VPs, Heads, Directors, Mangers of:

  • Clinical Supply Operations
  • Clinical Trials Logistics
  • Clinical/Investigational Supplies
  • Shipping and Distribution
  • Packaging and Labeling
  • Clinical Supplies Manufacturing
  • Compliance

About the Organizers:

Pharma IQ, a division of IQPC, provides useful training courses, conference and expositions for pharmaceutical executives to network and learn the latest pharma business development and trends occurring in organizations today. Pharma IQ focuses on establishing an interactive experience featuring practical, objective, and up to date insight from pharma industry leaders.

 

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