INTERPHEX and Pharmaceutical Processing announce INTERPHEX Live program.
International Pharmaceutical Expo (INTERPHEX), the premier event dedicated to pharmaceutical, biotechnology and device innovation, technology and knowledge from development through commercialization, and Pharmaceutical Processing, a leading provider of news and information on the cutting-edge technologies and services for the pharmaceutical, biopharmaceutical, nutraceutical, and medical device markets, have released the INTERPHEX Live program.
As the industry looks to reduce costs, increase productivity and maximize efficiency, the program was developed to address and deliver solutions for industry challenges by providing the latest in state-of-the-art technologies and access to industry expertise in a unique filmed format presenting reviews, interviews, and lively discussion. INTERPHEX takes place March 21-23, 2017 at the Javits Center in New York, New York.
“We are extremely pleased to have such a high caliber of expertise included within our exciting program, INTERPHEX Live,” said Melissa Ashley, Senior Vice President, INTERPHEX. “Our technology-focused three-day program offers industry professionals the opportunity to gain innovative solutions for compliant, flexible and cost-effective operations from industry experts. INTERPHEX continues to deliver innovation and excellence in pharmaceutical, biotechnology and device development and manufacturing.”
“On behalf of INTERPHEX and Pharmaceutical Processing, we are proud to offer even more value with this timely technical program,” said Todd Baker, General Manager, Manufacturing, Advantage Business Media. “INTERPHEX Live is a great no cost way to increase your knowledge and learn new operational efficiencies and Cost of Good strategies in a fun and entertaining format. Attendees and exhibitors have the opportunity to view the discussions live via our show floor studio as we broadcast throughout the show floor and record for ‘on-demand’ post-show viewing.”
INTERPHEX Live Schedule:
Moderated by Russ Somma, PhD, SommaTech Consulting
Tuesday, March 21, 2017
“Realizing Benefits and Efficiencies from Quality Systems” – 10:15am-11:00am
Aaron Weinstein, Sr. Director Validation Services, IPS-Integrated Project Services; Jeff Meltzer, VP of Quality Management, Trevania Inc.
“Evolution of Pre-filled Syringes” – 11:15am-12:00pm
Les Edwards, Vice President, Vice President, Technology and Business Development, SKAN US; Dan Schmidt, Director: Fill, Finish, Inspection and Packaging, Sanofi; Jared Shook, Director, Aseptic Processing Technology, IPS – Integrated Project Services
“Capsules: The Go-To Dosage Form”- 1:30pm-2:15pm
Jonathan Gilinski, SVP of Business Development, CapsCanada; Michael Vileikis, Technology Manager, Global Strategy and Technology, IPS-Integrated Project Services
“cGMP Clean Space: Innovative Solutions for Compliant and Cost-Effective Facilities” – 2:15pm-3:00pm
Ed Caulkins, Director of Facility Design, DME; Blake Hodess, President, Hodess Cleanroom Construction; Charlie Johnsrud, Principal, Johnsrud Architects; Tim Loughran, Consultant, Cleanroom Construction Associates
“Fortem: Challenges and Opportunities in Developing a New Plastic Film for Bioprocess Activities” – 3:00pm-3:45pm
Susan Burke, Staff Scientist, GE Healthcare; Ross Acucena, Product Strategy Manager, Bio Process , GE Healthcare; Parrish M. Galliher, Chief Technology Officer, BioProcess, GE Healthcare Life Sciences; Nicholas Berendt, Director of Global Medical Market Development, Sealed Air Medical
“The Future of Flexible Manufacturing” – 3:45pm-4:30pm
Jeff Odum, CPIP, Global Technology Partner, NNE Pharmaplan US
Wrap-up: Day 1 – 4:45pm-5:00pm
Wednesday, March 22, 2017
“DSCSA: New Regulations Require Action” – 10:15am-11:00am
Brian Daleiden, Vice President, Industry Marketing, TraceLink; Peter Sturtevant, Sr. Director Industry Development-Pharma, GS1 US
“Regulatory Aspects of Continuous BioProcessing” – 11:15am-12:00pm
Alice Redmond, Vice President, EU Operations and Head of Bio, Pharma & Medical Device Services, Commissioning Agents
“Serialization” – 1:30pm-2:15pm
Ashley Umberger, Manager of Engineering, Afton Scientific; Mark Wessel, Director Engineering-Global Serialization Program Leader, Pfizer CentreOne; Graham Clark, Director CMO/3PL Business, TraceLink; Christopher Howell, Senior Director, Global Engineering and Technology, Patheon
“Biosimilars 3.0” – 2:15pm- 3:00pm
Michiel E. Ultee, Ph.D., Principal, Ulteemit BioConsulting; Mani Krishnan, Vice President, Technical Services & Scientific Affairs, Pall Corporation
“Quality Metrics/Quality Agreements” – 3:00pm-3:45pm
Tom McGrath, Vice President of Quality, LSNE; Tom Thorpe, CEO, Afton Scientific; Scott Gunther, VP, Quality, Catalent
“Continuous Manufacturing Opportunities Keep Expanding in Pharma” – 3:45pm-4:30pm
Andrew Christofides, Technology Director, Process Equipment, Jacobs; Eric Jayjock, PhD, Director of Continuous Manufacturing, Patheon; Jay Jones, General Manager, Delavau; Fernando Muzzio, Distinguished Professor Chemical and Biochemical Engineering, Rutgers University
Wrap-up: Day 2 – 4:45pm-5:00pm
Thursday, March 23, 2017
“The Changing Regulatory Landscape: Looking from the Outside In” – 10:15am-11:00am
Joe McGinnis, Senior Regulatory Compliance Advisor, Johnson & Johnson
“Trends in Medical Device” – 11:15am-12:00pm
David Armbruster, Johnson & Johnson
Wrap-up: Day 3 – 12:00pm-12:15pm
A show planner tool is available by clicking here for attendees who wish to better plan their schedules and help with business networking. Registration for INTERPHEX is required. To register for INTERPHEX 2017, visit http://www.interphex.com/en/Register.
(Source: INTERPHEX)
