June 10 - 12, 2019 | California, United States

Main Conference Day Two

9:00 am - 9:45 am Bridge the Gap Panel Discussion: Mastering Import/Export Compliance for your Global, Multi-Layered Supply Chain

Travis Tibbetts - Global Distribution Manager, Pacira Pharmaceuticals
Daniela Vernille - Director of Temperature Control Logistics and Operational Compliance, Pfizer
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Travis Tibbetts

Global Distribution Manager
Pacira Pharmaceuticals

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Daniela Vernille

Director of Temperature Control Logistics and Operational Compliance
Pfizer

9:45 am - 10:30 am Reaching the 5th Child: How Technological Innovation & Industry Collaboration are Delivering Life Saving Vaccines to Children in Underdeveloped Nations

Harvey Rubin MD, Ph.D - Professor of Medicine, Microbiology and Computer Science and Founder & Director, University of Pennsylvania and Energize the Chain
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Harvey Rubin MD, Ph.D

Professor of Medicine, Microbiology and Computer Science and Founder & Director
University of Pennsylvania and Energize the Chain

11:15 am - 12:00 pm Preparing for Brexit Effects on the EU GDP Requirements and What it Means for your Global Supply Chain

12:00 pm - 12:45 pm Product Launch Efficiency: Collaboration Between Clinical, Commercial & Regulatory to Ensure Temperature Controlled Product Quality from Bench to Bedside

Track A- Cold Chain

1:50 pm - 2:30 pm Interactive In-Depth Discussion Lounges
Daniela Vernille - Director of Temperature Control Logistics and Operational Compliance, Pfizer
Table 1- Global GDP Discussion
Table 2- Defining Roles & Responsibilities in a Siloed Organization 
Table 3- Validating Packaging in the Last Mile
Table 4- Complying with Global Regulations for CRT Products
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Daniela Vernille

Director of Temperature Control Logistics and Operational Compliance
Pfizer

Track B- Clinical Trial Logistics

1:50 pm - 2:30 pm Utilizing Simulation Tools for Supply Planning and Demand Forecasting to Ensure On-time Delivery with Minimal Scrap

Track C- Pharma Traceability

1:50 pm - 2:30 pm Defining Operational Requirements For the Flow and Evaluation of ‘Exception” Handling Post Integration
Table 1- Regulatory Audits
Table 2- Shipping Between Temperature Extremes
Table 3- Emerging Market Infrastructure Challenges
Table 4- Shipping Outside of Label Claims
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Lou Sehl

Executive Director, Manufacturing and Technical Operations
MyoKardia

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Matthew Parker

Associate Director, Materials
Nektar Therapeutics

Track B- Clinical Trial Logistics

2:40 pm - 3:20 pm CASE STUDY: Advantages and Disadvantages of Phase Change Materials in Single Use and Reusable Containers for Transportation

Track C- Pharma Traceability

2:40 pm - 3:20 pm PANEL DISCUSSION: Partnering with the Right Partner: Addressing Complexities that Could Occur When Solidifying the Right Partner for Your Serialization Needs

Track A- Cold Chain

3:55 pm - 4:40 pm CASE STUDY: End-to-end Process Excellence to Ensure Uninterrupted Delivery & Minimize Risk
Eugenio Filippi - Associate Director Plasma Logistics & Analytics, Shire
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Eugenio Filippi

Associate Director Plasma Logistics & Analytics
Shire

Track B- Clinical Trial Logistics

3:55 pm - 4:40 pm Qualification of Thermal Shipping Systems to Meet Global Health Authority Requirements
Myriam Antoun - Director, Global Regulatory Affairs, PPD
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Myriam Antoun

Director, Global Regulatory Affairs
PPD

4:40 pm - 5:25 pm PANEL DISCUSSION- How the Industry can Collaborate to Create Standards & Methods for Cold Chain