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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.
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 |
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 |
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. |
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