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Pharmaceutical Supply Chain Summit 2012


June 6-7, 2012
Sheraton Baltimore North Hotel
Baltimore, MD
United States

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Conference Details:
Join experts and industry professionals from across the country, and across the value chain, for Opal events' 3rd Annual Pharmaceutical Supply Chain Summit!

This year's Pharmaceutical Supply Chain Summit will feature industry perspectives and real-world strategies for addressing issues such as: cold chain integrity across borders and resources, the impending deadlines for serialization and other global regulatory initiatives- and how to prepare, the emergence of biologics and their impact on the supply chain, sustainability and the new initiatives taken across the value chain and much more!

The 3rd Annual Pharmaceutical Supply Chain Summit will provide solutions for regulatory and compliance issues that affect pharmaceutical and medical device manufacturers, transportation companies, pharmacies, hospitals and patients. As recalls continue to plague the industry, drug safety and supply chain fidelity have become paramount. 
Who Will Attend:
Opal Events' Pharmaceutical Supply Chain Summit 2012 conference has been researched and developed specifically for drug and device manufacturers including Managers, Directors and VP's of: 
  • Research & Development
  • Packaging
  • Clinical Research
  • Supply Chain
  • Logistics
  • Distribution
  • Security
  • Global Logistics
  • Regulatory Affairs
  • Transportation
  • Risk Management
  • Engineering
This conference will also appeal to major pharmaceutical distributors, including pharmacy chains, hospitals, and patient care centers. Government officials, compliance officers, individuals from university and research institutes will also find much to benefit from in attending this comprehensive event.
Join Us For:
  • 15+ panels, discussions and presentations of the most relevant, pertinent information to the pharmaceutical and medical device supply chain
  • Stimulating discussions on the roles and responsibilities within the supply chain, as well as new and innovative technologies and strategies
  • One of the only conferences to highlight the importance of ambient drug regulations, and update the industry on the future of this landscape
  • 5+ hours of scheduled networking opportunities
Hotel Info:
TBA
Conference Registration Prices:
Early Bird Rate
(Expires 4/27/12)
Standard Rate
Service Providers
$795
$995
*Pharmaceutical/Medical Device Companies, Academia, Government, Non-Profit
First 100 Free, after $495

Register Now!

Group Discounts:
Register 3 people and receive 10% off ***
Register 4 people and receive 15% off ***
Register 5 people or more and receive 20% off ***

If you'd like to be invoiced, please submit your contact details on the registration page and select "Please invoice me" at the bottom of the page.

If you are interested in sponsorship, exhibiting, or speaking opportunities, please call 212-532-9898 or email information@opalevents.org
* TERMS & CONDITIONS
Subject to approval. To qualify you must be currently employed by a non-vendor company. Eligibility will be verified by conference producer. Opal reserves the right to allocate places and to refuse applications.

Registration price reflects $100 online discount
Media Sponsor:
Pharm Cast
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Past Attendees
Group Leader/Manager, Abbott Vascular Inc
Senior Packaging Engineer, Abbott Vascular Inc
Associate Director of Supply Chain and Logistics, Agennix
Managing Director, Alaska Airlines
Regional Cargo Sales Manager, Alaska Airlines
Senior Director Supply Chain, Alexion Pharmaceuticals Inc
Supply Chain Manager, ALK Abello
Managing Director, Alliance for Foam Packaging Recyclers (AFPR)
President & CEO, Alphagenics Inc.
VP Strategic Development, Alphagenics Inc.
VP New Product Research, Alphagenics Inc.
VP Market Development, Alphagenics Inc.
Product Sales Specialist, Bahnson Environmental Specialties
Product Sales Specialist, Bahnson Environmental Specialties
Global Demand and Supply Manager, Becton, Dickinson and Company
Sr. Business Director, Becton, Dickinson and Company
Packaging Engineer, Becton, Dickinson, and Company
Senior Packaging Engineer, Becton, Dickinson, and Company
Director, Quality Management and Regulatory Compliance, Becton, Dickinson and Company
General Manager, Berlinger
Manager Packaging Engineer, Boehringer-Ingelheim
Director, Boehringer-Ingelheim
Senior Packaging Engineering, Boston Scientific
Packaging Engineer, Boston Scientific
Packaging Engineer, Boston Scientific
Packaging Engineer, Bristol Myers Squibb
President and CEO, Cary Pharmaceuticals Corp
Technical Specialist Labeling, Celgene Corporation
CEO, Checkitin.org
Manager, Project Logistics, CoreRx Inc.
Director of Strategic Devo, Council of Supply Chain Management Professionals
Sales and Marketing Coordinator, CSC Laboratories
Global Market Manager, Packaging, DuPont Packaging and Industrial Polymers
Accounts Executive, Early Alert
Packaging Technology Team Leader, Eli Lilly
Regional Account Manager, Envirotainer
Commissioner’s Fellow, FDA
Consumer Safety Officer, FDA
Consumer Safety Officer, FDA
Public Health Analyst, FDA
Managing Director, Life Sciences & Specialty Services, Global Trade Services, FedEx Express
Vice President, Pharmaceutical Development, Femmepharma Global Healthcare Inc
Board Member, Florida Board of Pharmacy
Attorney, Fox Rothschild LLP
Vice President Reliability Solutions, Genesis Solutions
VP, Channel Strategy/Pharmacy Solutions, GlaxoSmithKline
Global Manager, GlaxoSmithKline
President, Gold and Domas Research
Senior Manager, Sustainable Packaging Coalition, GreenBlue
Vice President Marketing & Business Development, Haselmeier
Executive Director, Healthcare Compliance Packaging Council
Bioprocess Associate III, Human Genome Sciences
Sr. Device and Packaging Engineer, Human Genome Sciences
Senior Sterilization Scientist, Corporate Quality Systems, Integra LifeSciences Corporation
Vice President Quality Systems Compliance, Integra LifeSciences Corporation
Director, Quality Systems Compliance, Integra LifeSciences Corporation
Editor in Chief, International Pharmaceutical Quality
Senior Director, Supply Chain, Johns Hopkins Hospital
President, Lifoam Industries, LLC
VP of Operations, Lifoam Industries, LLC
VP of Sales, Lifoam Industries, LLC
Pharmacist Compliance Officer, Maryland State Board of Pharmacy
Consultant, McCune Consulting
Manager, Merck
Product Protection & Optimization Lead, Merck
Senior Engineer, Merck
Senior Packaging Engineer, Merck
Biologic Project Lead, Merck
Associate Professor, Michigan State University School of Packaging
Chief Operating Officer, Mobius Therapeutics, LLC
Program Manager, National Institute of Standards and Technology (NIST-MEP)
Executive Director, Niagara University
Director, Owens and Minor International
Senior Director, Supply Chain, Johns Hopkins Hospital, Owens and Minor International
Packaging & Sustainability Consultant, Packaging Development
CEO and Founder, Patients’ and Consumers’ Pharma
EVP, PBM Pharma
Product Engineer, Perrigo
Engineer, Pfizer
Director of Regulatory Affairs, Pfizer
Director, Global Conveyance Security, Pfizer
Senior Packaging Equipment Engineer, Pfizer
Manager, Global Master Data Management, Pfizer
Manager, Pfizer
Editor in Chief, Pharmaceutical Commerce
Supply Chain Manafer, Pharmathene
Consulting and Business Development, PIPS
Sales representative, Praxis Packaging
Sales representative, Praxis Packaging
Senior Consultant, PriceWaterhouseCoopers
Consulting and Business Development, Product Identification & Processing Systems, Inc.
VP Inspection Technologies, PTI Inspection Systems
Regulatory and Compliance Officer, Pulsecor
Manager, QA Compliance Operations North America, Qiagen
Quality Specialist III, Technical Operations New Product, QA Operations North America,
Qiagen
Manager, Quality Assurance and EHS Operations North America, Qiagen
Specialist II QA Supplier Quality Operations North America, Qiagen
Specialist II QA Supplier Quality Operations North America, Qiagen
Senior Team Leader Warehouse Ops Inv Admin Operations NA, Qiagen
Manager Tech Ops Prod Imp & Proj Mgt Operations NA, Quiagen
Manager Tech Ops Prod Imp & Proj Mgt Operations NA, Quiagen
Specialist II Prodn Plan Prodn Planner Operations NA, Qiagen
Manager Prodn Kit Assy Operations NA, Qiagen
VP Supply Chain Manager, Quiagen
QA Appliance Manager, Quiagen
Director, Quiagen
Director, Quiagen
Director, Quiagen
Director, Quiagen
Manager, Quiagen
Manager, Quiagen
Manager, Quiagen
Director Manufacturing and Logistics, Quinnova
Director, Global Supply Chain Management Program, Rider University
Supply Chain Validation Consultant, Roche Diagnostics Corporation
Medical Purchasing Supervisor, Royspec
Consultant, S4 Consulting
Director, S4 Consulting
Process Engingeer II, Sangart, Inc
Vice President National Accounts, SBA Global Logistics
Marketing Manager, SenseAware
Senior Manager Product Labeling and User Documentation, Siemens Healthcare
VP, Soliance
Senior Vice President, St. Barnabas Hospital
Senior Packaging Engingeer, St. Jude Medical
Director, Sustainable Supply Chain Foundation
Executive Vice President, The Mundy Companies
Senior Manager, The Mundy Companies
VP Business Development, The Mundy Companies
Assistant Branch Chief, TSA
Planner, UC Davis
Vice President, Sales, Uromed LLC
President, Van Bodegraven Associates
Attorney, Vinovations
Professor, Virginia Tech
Project Specialist, Package Development, West Pharmaceuticals
Project Engineer, West Pharmaceuticals
President, White and Company LLC
2012 Agenda (current as of 6/05/12)
Past Conference Day One: Wednesday, June 6, 2012
7:30 am
Continental Breakfast
8:15 am
Opal Events' Opening Remarks
8:20 am
Chair's Welcome and Audience Demographics
8:30 am
The Evolving Dynamics of Biopharma Supply Chain Management

While the global pharma market is expanding, with more shipments into emerging economies, the market in developed countries is moving rapidly toward specialty pharmaceuticals, requiring more customized distribution processes. And within the specialty pharma sector, the prevalence of cold-chain processes is significant. These dynamics will both create opportunities and obstacles to markets and business development. This presentation will review the macro trends, then focus on the dynamics of national and global temperature-sensitive shipping, based on the just-published 2012 edition of the Pharmaceutical Commerce Biopharma Cold Chain Sourcebook.

Nicholas Basta, founder and editor-in-chief, Pharmaceutical Commerce magazine
9:15 am
Global Network, Visibility, and Cold Chain Solutions – Keeping Cool with FedEx Healthcare Solutions
  • Commitment to the Healthcare Industry
  • Global Market Forces
  • Cold Chain Logistics at a Glance
  • Innovative Technologies
Richard Smith, Managing Director, Life Sciences and Specialty Services, FedEx Express
Fed Ex Md
10:15 am
Morning Refreshment & Networking Break
10:45 am
Crossing the Line: Bar Coding and the Supply Chain
  • Discuss how improvements in product, supply, and material management coordination can be achieved by use of bar codes. 
  • Discover ways of using barcodes for Unit-of-use items for inventory control/tracking
  • Learn techniques for using barcodes for tracking of reusable/refurbished equipment and supplies, product recalls, and warnings throughout the entire chain
  • Implement test labels to ensure labeling accuracy
  • Identify best Practices for using Bar codes on high-usage drugs so systems can easily and quickly address the most prominent threats to patient safety
William E. McCune, DrPH, CPP, Consultant, McCune/ Consulting
George Wright IV, VP, Consulting and Business Development, Product Identification & Processing Systems Inc
Delmar R Mineard, Manager Packaging Engineer, Boehringer-Ingelheim
11:45 am
Systems Based Design of Domestic and Global Supply Chains
  • Discover how all three of these basic components of the global supply chain mechanically interact during storage and distribution
  • Learn to improve supply chain efficiency, implement a fundamental shift from the current component by component design to a true systems based design methodology
  • Analyze new, user friendly, design technologies have been developed which model these interactions and when used by trained packaging and logistics professionals, significant improvements in supply chain operating efficiencies are possible.
Marshall S. White, PhD, President, White and Company LLC
Jack T. Ampuja
, Executive in Residence, Niagara University
12:40 pm
Temperature Monitoring, Mapping & Secure Transport
  • SenseAware powered by FedEx provides near real-time information, exposure to light, relative humidity, and barometric pressure throughout the shipment journey
  • Permitted by the Federal Aviation Administration (FAA)
  • Customizable alerts can be set and will provide a notification if a package exceeds their preset limits
  • All of this information can be shared continuously with invited participants through a feature-rich web-based platform
Chris Swearingen, Marketing Manager, SenseAware
1:15 pm
Luncheon
2:25 pm
Frameworks To Assure Integrated Strategic, Tactical and Operational Supply Chain Planning and Management
  • Identify the current commercial and clinical outsourced production environment in Life Sciences Business
  • Determine the operational and information challenges created as production is outsourced
  • Apply the collaborative business network architecture required to ensure visibility, accountability and control across external supply relationships
  • Outline the responsibilities of the CMO and CPO in the pharmaceutical contract manufacturing relationship
Tan Miller, Director, Global Supply Chain Management Program, Rider University College of Business Administration
3:00 pm
Afternoon Refreshment & Networking Break
3:30 pm
Asset Management: A Supply Chain Value Proposition for Gaining Competitive Advantage
  • Linking Maintenance to achieving Operational Excellence
  • Reducing cycle time and conversion costs
  • Improve visibility to packaging at every point in the supply chain
  • Converting Maintenance from a Cost Center to a Competitive Advantage
  • minimize loss and optimize supply chain efficiency
  • Six Sigma Process for developing an Asset Management Master Plan

John Rocco, Executive Vice President, The Mundy Companies
Michael Greenholtz, Vice President Reliability Solutions, Genesis Solutions
Mike Mills, Senior Manager, Mundy Companies

The Mundy Companies
4:30 pm
Roundtable Workshops
  • Attend 2 half hour long workshops and join other industry leaders as they host in-depth discussions on a variety of topics
  • After 30 minutes, attendees will be given the opportunity to switch rooms and hear from a different industry leader on a while new topic
  • Remember to sign up for your workshop early to ensure your seat!!! Each workshop will be hosted in a separate room

START-UPS AND SHUT-DOWNS – AN INTEGRATED SERVICES APPROACH TO SAVING MONEY AND MAXIMIZING PRODUCTION DAYS

  • Planned stoppage in production for:
    • Routine maintenance
    • Construction or facility modifications
    • Major installations
    • Validation testing
    • Other tasks
  • Extensive planned engineering followed by a short period of rapid execution
  • Startup of manufacturing afterwards

Mike Mills, Senior Manager, Mundy Companies
Joe Rettinger
, VP, Soliance
The Mundy Companies
Health Care Logistics in Alaska: Collaboration between rural communities and industry, a Rx that works.

  • Alaska is home to 229 federally recognized tribes and 130,000 Alaska natives, about 85,000 of whom live in rural villages reachable only by boat, plane, snow machine or dog sled. 
  • Since 1970, Alaska Natives have increasingly assumed more responsibility for managing their own health care through the Alaska Tribal Health System (ATHS) and the Alaska Native Tribal Health Consortium (ANTHC)
  • The combined efforts of industry, the ATHS and ANTHC have helped tackle health care logistics challenges to ensure the safe and timely delivery of crucial supplies, samples and materials to remote village locations
Joe Samudovsky, Managing Director, Alaska Airlines
Alaska Air Cargo
5:30 pm
Day One Closing Remarks and Mundy Presents a Cocktail Reception (in the Exhibit Hall)
The Mundy Companies
Past Conference Day Two: Thursday, June 7, 2012
7:15 am
Continental Breakfast & Registration
8:00 am
Chair's Welcome and Day One Re-Cap

Richard J. Sherman, Director of Strategic Development, Council of Supply Chain Management Professionals
8:05 am
TSA Update on the Certified Cargo Screening Program
  • Hear a comprehensive overview of the International inbound screening plans
  • Create a certified plan to meet the 100% screening mandate in the supply chain
  • Learn strategies for design and development in accordance with these regulations
Gary E. Lupinacci, Assistant Branch Chief, Certified Cargo Screening Program, TSA/TSNM
9:00 am
Ocean Freight Services Streamlining Your Supply Chain
  • Analyze the benefits of Sea travel for your supply chain
  • Discuss the expansion of the Panama Canal to allow larger vessel transport
  • Examine the increased security and temperature control in sea travel
Brad Elrod, Director, Global Conveyance Security, Pfizer Global Logistics Compliance
10:30 am
Global Supply Chain Management in the "Smart World"
  • Learn what's driving "smart" transformation in the Supply Chain
  • Develop performace improvement intiatives to drive profitable growth
  • Hear how different industries are performing based on benchmarking and current research
  • Understand how supply chain performance impacts financial performace
  • Take away a game plan to launch your journey to supply chain excellence
Richard J Sherman, Director of Strategic Development, Council of Supply Chain Management Professionals
10:45 am
Morning Refreshment & Networking Break
11:15 am
Megatrends in the Industry and how they effect your Supply Chain
  • A discussion of four megatrends in the industry and their impacts on supply chain planning and operationsfrom two professionals deep in the industry
  • Topics discussed with include; ships in transit modes, the emergence of air movements, the challenges in roadway distribution, new inventory consequences of physically longer supply chains, point of application distribution leading to higher inventory storage, and electronic innovations in the past six years that are changing the cost of distribution.
Art van Bodegraven, President, Van Bodegraven Associates
Jack Fish
, VP, Channel Strategy/Pharmacy Solutions, GlaxoSmithKline
12:00 pm
Understanding Users Needs Through Simulation: Michigan State's Medical Simulation Program
  • Industry focus is shifting from protecting the product to protecting the patient
  • More therapies are being applied by the patient and a quickly growing geriatric population- packaging needs to keep up with these developments
  • Learn how Michigan State's simulated 'hospital' is allowing students to look critically at how packaging issued, (and misused), in real-world settings, and what the industry has learned from their tests
Dr. Laura Bix, Associate Professor, Michigan State University School of Packaging
12:45 pm
The Last Mile: From Pharmacist to Patient
  • Prepare for the new ways drugs are being handled and administered in pharmacies
  • Learn to navigate the difference in regulatory standards when moving from Distribution to Neighborhood
  • Pharmacy territory, and develop systems compliant with both
  • Implement Strategies for incorporating Pharmacies and Patients into Your Supply Chain
  • Determine how distribution should handle working with pharmacy chains networks
Walter Berghahn, President, SmartRmeds for Life, Executive Director, HCPC
1:30 pm
Utilizing Emerging Technologies in Pharmaceutical Delivery
  • New package delivery systems increase package integrity challenges. New technologies are required to determine package integrity of complex delivery systems.
  • Container closure integrity is growing in importance with respect to package distribution. Deploying more accurate, reliable, and quantitative methods for determining package integrity increase control of product released for distribution.
Reid Graves, Senior Pharmaceutical Advisor, 6DCP
Oliver Stauffer,
VP Inspection Technologies, PTI Inspection Systems
2:30 pm
Conference Adjourns
Speaker Biographies
Jack T. Ampuja, Executive in Residence, Niagara University

Mr. Ampuja has over 30 years of supply chain management experience with five Fortune 500 firms. He served as Senior Vice President of Operations at a multi-billion dollar international company heading up a $200 million division. He has presented for the US Agency for International Development and testified before U.S. Congress as a transportation expert. Mr. Ampuja has been featured on the cover of Logistics Management magazine.

Mr. Ampuja is certified by the American Society of Transportation and Logistics, and the National Association of Purchasing Management. He has served as Co-Chairman of the Canadian American Border Trade Alliance Transportation Committee for five years and on the Logistics Committee of the Grocery Manufacturers of America for over ten years. Currently, Mr. Ampuja serves on the editorial advisory board for Supply Chain Management Review, the Business School Dean' s Council at the University of Massachusetts, is Co-Chair of the Logistics Council for Buffalo Niagara Partnership (Chamber of Commerce) and Chair of the Western New York Roundtable for Council of Supply Chain Management Professionals. Additionally, Mr. Ampuja serves as the Executive Director for the Center for Supply Chain Excellence at Niagara University and the President of Supply Chain Optimizers.

Mr. Ampuja has a BS degree in business administration from the University of Massachusetts, a year of post graduate study in transportation at Northeastern University, and an MBA degree from the University of Connecticut.

Dr. Laura Bix, Associate Professor, Michigan State University School of Packaging

Dr. Bix is an Associate Professor at the School of Packaging at Michigan State University. She specializes in healthcare packaging at the School, where she has taught: Principles of Packaging, Plastics and Packaging, Packaging Design and Development, Medical Packaging, Packaging Laws and Regulations and Scientific Writing. In 2007, she was the recipient of the CANR New Teacher Excellence in Teaching Award.

Dr. Bix has served as the Vice-Chair of ASTM Committee D10.32, the Committee on Consumer, Pharmaceutical and Medical Packaging, from 2004-2008, and as a member of ASTM Committee F-02, since 2002. In 2008, she was named one of the Medical Device Industry's most notable people by Medical Device and Diagnostic Industry magazine.

She is also a member of the Institute of Packaging Professionals and the RCA Include Network, and has recently been designated as the US expert on ISO/TC 122, a guideline aimed at creating inclusionary packaging.

She is on the editorial boards of The Journal of Testing and Evaluation (West Conshohocken, PA) and Pharmaceutical and Medical Packaging News (Los Angeles, CA), as well as the advisory boards of Shelf Impact! (Chicago, IL) and Medical Device Developments (Nottingham, UK) She is currently an executive leader Philips Healthcare, Royal Dutch Philips, based in Amsterdam, The Netherlands and the U.S. and is an international published author and speaker on business intelligence, competitive, market intelligence and marketing, strategic planning and the application of these to business functions.

Art van Bodegraven, President, Van Bodegraven Associates

Art van Bodegegraven, Supply Chain Practice Leader for S4 is a 40+ year consulting veteran, with the last 20 focused exclusively on Logistics and Supply Chain Management. His prior experience includes: Partner, The Progress Group; Managing Director, Coopers & Lybrand Consulting; Chairman, The Supply Chain Group; and, President, Van Bodegraven Associates. He is a graduate of Purdue University.

A prolific speaker, writer, blogger, and educator, he also leads curriculum and faculty development for CSCMP workshop programs, supports the MBLE program at The Ohio State University, and previously worked closely with Georgia Tech's Supply Chain and Logistics Institute.

Art's current professional interests are centered on the powerful role of culture and business relationships in building sustainable high-performing supply chains.


Jack Fish, VP, Channel Strategy/Pharmacy Solutions, GlaxoSmithKline

Jack brings over 30 years of experience in the health care industry with expertise in executive leadership and management, sales leadership with P&L responsibility, managing national accounts, as well as strategic planning.

Jack spent over 33 years at the Senior Executive Level of GlaxoSmithKline (US) in Sales Management, Sales Support Management, Wholesaler and Pharmacy Relations, and in Channel Management and Pharmacy Solutions. Jack began his career at GlaxoSmithKline in 1976 as a Sales Representative and grew with the company in the changing landscape of the health care industry.

Jack has served on the Board of Directors for the National Association of Chain Drug Store Foundation (NACDS) from 2004-2009, and served as the Vice Chairman of the Pharmacy Industry Council. From 2005-2009, he served on the Board of Directors of the Pharmacy Quality Alliance (PQA).

In 2006, he received the Lifetime Achievement Recognition- Nexus Award presented by the Healthcare Distrubution management Association (HDMA). In 2009, he received the Lifetime Achievement Award - Harold W. Pratt Award, presented by the National Association of Chain Drug Stores (NACDS).

His assignments took him from New York to Boston, Dallas, and finally to Philadelphia in 1989. He ended his tenure with GSK as the Vice President for Channel Management and Pharmacy Solutions in 2009.

Jack Fish received his bachelor's degree from Syracuse University in 1968.

Reid Graves, Senior Pharmaceutical Advisor, 6DCP

Reid H. Graves served at Merck & Co., Inc. for 33 years in a wide variety of responsibilities. Most recently, he was the Senior Business Lead for Supply Chain Master Data. Reid led the SAP Supply Chain Master Data team responsible for the global blueprint of Merck's ERP system. He built several custom web-based systems managing worldwide sales, inventory, and value chains for end-to-end supply chain management. He directed the global Inventory Management program for Merck's Manufacturing Division ($1.8 billion) resulting in demonstrated supply chain improvements. Reid has a Master's degree in Biology from the College of William and Mary in Virginia. He currently serves on the Advisory Board for 20/20 Pharma magazine.

Gary Lupinacci, Assistant Branch Chief, Certified Cargo Screening Program TSA

Mr. Lupinacci joined the Transportation Security Administration in 2008 after a long career in the private aviation sector. His role with the TSA is to play in integral part in rolling out the CCSF program, specifically as it relates to the Independent Cargo Screening Facility component and vertical industries.

In July of 2002, he joined Worldwide Flight Services. His responsibilities included overseeing the Health & Safety, Aviation Security, and TSA Compliance concerns for the North American cargo division. His duties as a Managing Director included financial and operational responsibility for WFS cargo cities.

Before joining Worldwide Flight Services, Mr. Lupinacci spent seven years with British Airways holding a number of management positions. His roles included Cargo Manager for the JFK operation, Director of Service Delivery for the Latin American market and lastly, Director of Customer Service East USA. In this role he held operational and fiscal responsibility for eleven online cities.

Prior to his time with British Airways, Mr. Lupinacci spent 23 years with Japan Airlines. He held a diverse blend of positions with JAL that encompassed both ramp and cargo operations.

Mr. Lupinacci served on the Board of Directors for the Florida Cargo Security Council and is a member of the International Cargo Security Council.

William E. McCune, DrPH, CPP, Consultant, McCune Consulting

William E. McCune, Doctor of Public Health and Certified Packaging Professional, has over 25 years of department leadership, innovation, and patents for healthcare package engineering and label design with several Fortune 500 companies. Direct reporting area has been in both R&D and Operations with key responsibilities to Quality, Regulatory, Marketing, Sales, and Legal. Healthcare products have included Rx, OTC, and diagnostic for both human and veterinary use as well as household and food products.

McCune's Doctoral Dissertation addressed the critical and in depth relationship of Public Health policy and packaging from primary stability to protective aspects needed for CR, TE, and prevention of counterfeits.

Personal hands on experience has been with test method development in the lab, actual lab construction, line optimization and new line installation, container design for unique functional improvements, and package/formulation testing for microbial, chemical, and leak properties. Key to success has been leadership ability to identify the essentials for priori tization within a project and also priority changes across multiple projects.

McCune is innovative and energetic with both individual company and across industry efforts for efficiency and regulatory compliance. Efforts have required ongoing involvement with FDA, CPSC, USP as Expert Committee Member, SPI in support of USP efforts, ASTM, ISTA, IATA, and colleagues in other pharmaceutical companies. Bill has also led full NDA and MAA product teams and worked with the full range of packaging materials and processes.

Most rewarding career successes resulted from innovative contributions, including patents, in the areas of operations improvements, total package problem solving for primary through POP, complex package issues for product chemical stability, implementation of novel aspects in packaging, and a graphics computer program that was utilized at NASDAQ.

McCune identifies new opportunities for successes in packaging to be presented by ongoing evolutionary needs in areas such as sustainability, enhanced bar codes, patient compliance, counterfeit prevention, and beyond. In the past equally difficult challenges were met with efforts for CR, UPC, cGMP, TE, and needle stick protection.

Tan Miller, Director, Global Supply Chain Management Program, Rider University College of Business Administration

Tan Miller is the Director of the Global Supply Chain Management program in the College of Business Administration at Rider University. Previously he worked in private industry for over 20 years where most recently he was responsible for the operations of J&J's US Consumer Distribution Network. Prior to that, he headed the U.S. Consumer Healthcare Logistics Network of Pfizer Inc., and he has also held production and distribution management positions with Mercer Management Consulting, Unisys, and American Olean Tile Company. Tan has published four books and over fifty articles, and has made over 100 industry and academic conference presentations on supply chain and logistics operations and planning. His two most recent books are titled Hierarchical Operations And Supply Chain Planning (Springer-Verlag Publishers) and Strategic Logistics: Efficient Transportation Decisions (Boskage Commerce Publications). Tan has also previously taught part-time in the MBA program of Villanova University, has guest lectured regularly at other universities and industry conferences, and has served on the editorial and advisory boards of a number of trade and educational journals and councils. Tan received an M.A, M.B.A and Ph.D from the University of Pennsylvania.

John Rocco, Executive Vice President, The Mundy Companies

John M. Rocco currently serves as Executive Vice President, Mundy Companies of Houston, Texas. In addition to business development, he has direct responsibility for the Mundy PharmaTech Division and Mundy Caribe LLC. Before joining the Mundy Companies, John was a member of Bayer’s senior management team in the USA until his retirement in 2006. As Vice President, Bayer Material Science LLC and General Plant Manager, he was responsible for Bayer’s largest multi-business chemical manufacturing complex in the Americas.

Previous positions included Vice President, Technical Operations USA with responsibility for multi-site pharmaceutical, biological and chemical manufacturing operations in the USA ; Vice President, Manufacturing, Rubber and Rubber Chemicals USA, and Director, Manufacturing for Animal Health Products.

Before joining Bayer, John served in various levels of manufacturing operations and financial management within Pfizer, Inc from 1978 to 1995.

John has been principally responsible for manufacturing strategy and operations, including manufacturing support operations. He has led successful strategy implementations in a number of key change management, productivity improvement and cost reduction efforts. These include pursuit of the Malcolm Baldridge Award and Class A Manufacturing at Pfizer, as well as Operational Excellence and SAP implementation at Bayer. In each case, productivity improvement, team work development, safety consciousness, cost reduction, asset utilization, culture change, and competitive advantage were key deliverables in positioning for world class manufacturing status.

John holds a BS Engineering degree from the U.S. Military Academy at West Point and received his EMBA from Columbia University in New York. He is an Army veteran and retired Colonel.

Marshall S White, PhD, President, White and Company LLC

MARSHALL S. ( MARK) WHITE, President of White and Company LLC. White and Company LLC is a consulting and software development company specializing in pallet, packaging, and unit load design. Dr White is also Professor Emeritus at Virginia Polytechnic Institute and State University, Blacksburg, Virginia, and a graduate of Colorado State University and Virginia Tech with B.S., M.S. and Ph.D. degrees. He taught graduate and undergraduate courses in the Packaging Science option and served as Director of the Center for Unit Load Design and The Pallet & Container Research Laboratory. He was responsible for the research, technical assistance and educational programs offered by the Center on behalf of the pallet, packaging and container manufacturers and user industries. The main thrust of these efforts has been the investigation of the relationship between the design of unit loads and their performance during storage and distribution of consumer and industrial products. The focus is on studying the dynamic and static mechanical interactions between packaging, pallets and unit load handling equipment. He has published widely on the subject of CAD/CAM design of pallets and containers and the dynamic sequence of palletized unit-loads in shipping environments. Dr White was recognized by Modern Materials Handling Magazine as one of the Top Ten Materials Handling Professionals for his revolutionary ideas on the "Systems-Based" alternative to the existing "component based design" of Global supply chains. Dr. White is a member of The Institute of Packaging Professionals, and the American Society of Testing and Materials D-10 Committee on Packaging. In this latter organization, he is a leader of the pallet Testing Task Group. He has also served as Head of the U.S. Delegation to the International Standards Organization TC-51 Committee on Pallets, and past Chairman of the MHIA, MH1 Committee on Pallets Standards

Oliver Stauffer, VP Inspection Technologies, PTI Inspection Systems

Oliver Stauffer received his Bachelors of Science degree from the University of Michigan and completed his MBA at Georgetown University - The McDonough School of Business. He worked for several years in analytical and R & D laboratories. His expertise and focus has primarily been new technologies and test method development specific to package testing. Stauffer joined PTI in 2005 as a member of the research and development team working on non-destructive testing of blister packaging. In 2006, he joined the sales team as sales/applications engineer for PTI Inspection Systems. He held the position of International Business Development Manager for PTI through 2010, focusing on global quality solutions for package inspection that are robust, faster, cleaner, cheaper to maintain, and that reduce manufacturing waste. In 2011, he was appointed as V.P. Inspection Technologies.

Richard J. Sherman, Director of Strategic Development, Council of Supply Chain Management Professionals

Rich Sherman is an internationally recognized pundit on trends and issues across supply chain management. He is currently Director of Strategic Development for the Council of Supply Chain Management Professionals (CSCMP). As a research director, he successfully launched the supply chain advisory services for AMR Research and lead in the development the SCOR model, founding the Supply Chain Council and serving on its Board. Throughout his career, Mr. Sherman has held senior management positions with visionary technology firms such as EXE, Syncra, and Numetrix, and marketing leading corporations such as Microsoft, IRI, Mercer Management Consulting, DEC, and Unisys serving clients globally. He has contributed scores of articles and speaks frequently on supply chain capabilities. Rich received his BA and MA from Notre Dame.


Richard Smith, Managing Director- Life Sciences and Specialty Services, FedEx Express

Richard Smith has a deep understanding of the valuable role logistics serve in connecting people and goods and creating economic growth. As the son of FedEx founder Frederick W. Smith, he literally grew up with the business watching FedEx evolve from an express shipping company to a worldwide portfolio of services. In his role as Managing Director of Life Sciences & Specialty Services, Smith provides strategic direction for developing customized logistics and supporting specialized services.

Smith joined FedEx Services in 2005 as a Senior Solutions Analyst. In 2007 he was promoted to Manager of Supply Chain Solutions, responsible for FedEx SupplyChain. In 2009 he was promoted to Managing Director of Life Science and Specialty Services.

Smith earned his undergraduate degree from George Washington University and his Juris Doctor from the University of Mississippi School of Law. He serves on the following Boards: Greater Memphis Chamber, LeBonheur Children's Hospital Foundation, and Blue Streak Scholarship Fund. 

George Wright IV, VP, Consulting and Business Development, Product Identification & Processing Systems Inc

George Wright IV is vice-president, consulting & business development, of Product Identification & Processing Systems, Inc. (PIPS) and a “second-generation” bar code expert with nearly 30 years of experience in the field. George serves as vice-chair of the AIM Unique Device Identification committee, past chair of AIM’s Technical Symbology Committee (TSC) and an active member of the U.S. Technical Advisory Group (TAG) to ISO’s SC31, the international standards body responsible for automatic identification standards. He is also a member of several GS1 work groups, including Bar Codes and Identification (BCID) and the Global Standards Management Process (GSMP) team, which reviews and votes on all change requests to the GS1 General Specifications. PIPS is a GS1 US Solution Partner; and George is one of three certified GS1 US Bar Code Consultants at the firm.

George holds 4 patents relating to automatic identification technology, including bar code print quality verification, an area in which he and his firm are considered industry leaders. George is a regular contributor to Pharmaceutical & medical Packaging News and has spent much of the last 10 years focused on bar coding in healthcare, with an emphasis on bar code implementation and quality systems in pharmaceutical and medical/surgical manufacturing. PIPS counts among its customers many of the top 20 global pharmaceutical and med/surg manufacturers, who rely on their expertise to guide them in correctly implementing GS1 standards and complying with FDA bar code rules. Among other projects, George was engaged as the principal subject matter expert and editor of the 2005 and the 2010 revision to the HDMA Guidelines for Bar Coding in the Pharmaceutical Products Supply Chain.

In 2004, George was recognized for his dedication and many contributions to the AIDC industry by his election to the AIDC 100, a peer organization of individuals who have made significant contributions to the growth and advancement of the Automatic Identification & Data Capture industry. Membership in the organization is limited to 100 individuals active in the industry and is a "Who’s Who" of the leading educators and innovators in AIDC today.

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