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2015 Pharma EXPO agenda

View the full 2015 Pharma EXPO Conference Program

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The Pharma EXPO Conference Program is the most efficient and effective way for you to get up to speed on:

  • Best practices for pharmaceutical manufacturing
  • The latest technological and regulatory trends
  • Practical applications of science and technology

This world-class program is organized by the renowned International Society for Pharmaceutical Engineering (ISPE), global leader in pharmaceutical manufacturing solutions, and designed to meet your needs.

Please note: This conference program is subject to change. Please visit www.pharmaexpo.com for updates and full conference information.

Monday, September 28 - MANUFACTURING OPERATIONS
9:00 am - 9:50 am Single Use Systems: Explore the Manufacturing Impact from Supplier Qualification to Optimizing Operations - Jeff
Odum, CPIP, SME, Director of Operations, IPS-Integrated Project Services, Inc.
9:50 am - 10:00 am Break
10:00 am - 10:50 am ISO 55000 and OEMs: Finding OEMs Who Can Offer Reliability Through Innovative Automation - Marie Getsug,
Senior Consultant, Maintenance & Reliability Services, CAI - Commissioning Agents, Inc.
10:50 am - 11:00 am Break
11:00 am - 11:50 am Spotlight Session:
Manufacturing Excellence: Empower Employees to Unleash Their Potential in High Performance Work Teams -
Steve Speer, Director, Operations, ProPharma Group
11:50 am - 1:00 pm Lunch
1:00 pm - 1:50 pm Microbial Contamination: An Audit Approach to Address Contamination in Process Equipment - Elizabeth Rivera,
Technical Services Manager, STERIS Corp
1:50 pm - 2:00 pm Break
2:00 pm - 2:50 pm Outsourcing Dilemma: Find the Right CMO to Minimize the Risk and Maximize the Quality of Your Brand - Kevin M.
Debbs, Process Specialist, CRB and Christa Myers, Associate/Lead Process Engineer, CRB

 

Tuesday, September 29 - COMPLIANCE TRENDS
9:00 am - 9:50 am Serialization and Track & Trace: From Theory to Practical Application Success Including Global Trends - Marcelo
Decanio De Oliveira, Validation and Consultancy Manager, NORDIKA
9:50 am - 10:00 am Break
10:00 am - 10:50 am Managing Risk of Cross Contamination for Multiple Product Facilities: Dedication, Segregation or Other? - George
Petroka, Principal, IES Engineers (Invited)
10:50 am - 11:00 am Break
11:00 am - 11:50 am Spotlight Session:
Quality Risk Management: Evaluating Compliance for Multiproduct Manufacturing and Inventory Facilities - Paul H.
Ahlijanian, Senior Manager, Pfizer, Inc.
11:50 am - 1:00 pm Lunch
1:00 pm - 1:50 pm The Process Lifecycle Model: A New Approach to Cleaning Validation - Elizabeth Rivera, Technical Services
Manager, STERIS Corp
1:50 pm - 2:00 pm Break
2:00 pm - 2:50 pm Finding The Root Cause: Utilizing Risk Management to Develop a More Robust Incident Investigation Model -
Pedro Dominguez, Senior Consultant, Malcom Associates and Chuck Krumwiede, Vice President, Malcom
Associates

 

Wednesday, September 30 - PHARMACEUTICAL PACKAGING
9:00 am - 9:50 am Optimized Packaging Lines: Reduce Engineering Time with Integrated System Diagnostics - Pamela Docherty, Life
Sciences Industry Manager - USA, Siemens
9:50 am - 10:00 am Break
10:00 am - 10:50 am Container Closure Integrity Testing for Blow/Fill/Seal: Reliability and Validation at Production Speeds - Marco
Renggli, Area Sales Manager, WILCO AG
10:50 am - 11:00 am Break
11:00 am - 11:50 am Spotlight Session:
Using Advanced Stability Modeling to Push Innovation and Speed to Market for Package Development - Kenneth
Waterman, PhD, President, FreeThink Technologies, Inc.
11:50 am - 1:00 pm Lunch
1:00 pm - 1:50 pm Materials Science: Case Study for Rational Design of Transdermal Patch Packaging - Georgia Mohr, Marketing
Director, Bemis Healthcare Packaging
1:50 pm - 2:00 pm Break
2:00 pm - 2:50 pm Oral Solid Dose Packaging: Assessing, Minimizing and Monitoring the Risk of API Exposure - Kevin Swartz, Senior
Engineer, IPS-Integrated Project Services, Inc.

 

>> For more information, click  here

 

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