The customized conference content of INTERPHEX 2013 is the product of group thinking carried out in a structured environment, which we refer to glibly as the advisory board. When you ask 15 industry professionals (the board) from across all sectors of our industry, you are guaranteed of getting valued input as well as things that are current and need to be addressed. The five conference tracks—regulatory quality assurance/quality control, product development, facility and process design, manufacturing and packaging, and supply chain—were pressure tested at INTERPHEX 2012 and have been leveraged effectively here for INTERPHEX 2013. Current Development Best Practices for IR and MR Dosage Forms will be discussed by Glenn Van Buskirk and will touch upon aspects of the current effort to address the needed updates for FDA guidance in the area of post-approval changes. The industry has regularly used the Scale-Up and Post-Approval Change (SUPAC) guidances that were issued more than a decade ago. The widespread use of these guidances along with current industry need has brought about a rethinking in this area and will produce a work product that will be a reliable and time-proven asset.
A keynote address, Reorganizing for the Future: Succeeding in the New Pharmaceutical Industry, will be given by Rajesh Nair from his perspective as president of Indegene. With a track record of having worked and consulted for many firms, Indegene has assisted various companies as they navigate through strategies to become more agile as they bring products to market and leverage existing product lines through a successful lifecycle.A team from Duquesne University lead by Jim Drennen and Benoit Inge has assembled a must-see session that will take the attendee through a practical utilization of aspects of quality by design as well as the application of key process control tools such as PAT. This will be followed by a panel discussion lead by Carl Anderson, also from Duquesne University. The panel will be case study-driven with experts from regulatory, development, quality, and the consulting sectors. The panelists will share their views as well as address must-have answers from attendees.
Combination products along with information-rich case studies will be presented from leading medical device manufacturers. David Armbruster from DePuy Synthes and Roy Fennimore from Johnson & Johnson will walk the attendees through each of their sessions. David will discuss the aspects of product realization from concept through manufacture while Roy will detail technology transfer for design control of convergent products.
A high priority has been placed on the “meeting place” that allows professionals to gather and exchange ideas. As highlighted by Bob Stewart, “there is a need to connect, face-to-face, in order to teach, to learn, to do business and to know each other better. Personal collaboration is critical to the industry INTERPHEX serves, and collaboration can begin with a conversation, with a meeting.” INTERPHEX has established just such a meeting place and forum.
The INTERPHEX team looks forward to meeting you at the Javits Center in New York City on April 23–25, 2103. Let us know your thoughts, at any time. We intend to serve the industry and continue our mission to make INTERPHEX the venue to learn it, hear it, see it, touch it, and procure it.