ISPE/FDA/PQRI Quality Manufacturing Conference, 5-7 June, Marriott Crystal Gateway Hotel, Arlington, VA

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Looking for ways to promote the 2017 ISPE/FDA/PQRI Quality Manufacturing Conference? Want to add a graphic to your website or newsletter? Need assist in getting approval to attend from your boss? Networking tips? We've got everything you need to make your conference experience a success.

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Networking

Here are some tips for making the most of your networking interactions before, during, and after the conference.

  • Have a concrete plan for your networking activities in mind. Coordinate your plan and your itinerary with other members of your team. Take advantage of the group registration discounts available.
  • Know who is attending. The delegate roster will be available to registered attendees on the workshop website one week before the event.
  • Reach out to individuals with whom you would like to connect via LinkedIn or other social media networks, prior to the workshop.
  • When you exchange business cards with new colleagues, make notes on the back for future reference. It helps to remember the context and your conversation after the conference is over.

Don't forget to bring your business cards!


Event Sponsors

Industry and Regulatory Experts to Discuss These Questions and More!

  • Could the concepts behind continuous process verification be similarly applied to maintain qualified state?
  • How can lifecycle quality management concepts be applied to Legacy products?
  • What major components are essential to establish a reliable state of process controls?
  • How much data is required to ensure that process is in state of control?
  • What are some successful scenarios for accelerated development products?
  • How can companies ensure a successful PAI on a new technology?
  • Should clinical studies be designed to include variability in product?
  • What validation variations are inherent with respect to sterile and non-sterile environments?
  • Are there viable alternate options for the implementation of quality metrics?
  • What are the key factors in managing control strategies for emerging technologies?
  • How and when are quality attributes defined as “critical”?
  • What are the most meaningful and predictive metrics?
  • Is FDA and MHRA approval required for manufacturing New Chemical Entity (NCE) or New Drug substance meant for clinical trials?

Submit Your Questions or Issues Now »


Keynote Speakers

Helen Saccone Photograph
US-EU Mutual Recognition Agreement
Helen Saccone, CDR, PharmD
Associate Director, Global Regulatory Policy
FDA/OC/OGROP
Michael Kopcha Photograph
Office of Pharmaceutical Quality Progress Update
Michael Kopcha, PhD, RPh
Director, Office of Pharmaceutical Quality, FDA/CDER
Thomas Cosgrove Photograph
Outsourcing Quality: Perspectives on Risk in the Global Drug Supply Chain
Thomas Cosgrove, JD
Director, Office of Manufacturing Quality
FDA/CDER/OC
François Sallans Photograph
Quality and Innovation: The Johnson & Johnson Experience
François Sallans, PharmD
Vice President, Quality & Compliance, Chief Quality Officer
Johnson & Johnson
Roger Nosal Photograph
The New Quality Paradigm
Roger Nosal, PhD
Vice President & Head of Global Chemistry, Manufacturing & Controls, Pfizer Inc.
Brian Boyd Photograph
Facility Management Past, Present, and Future: Transforming with the Times
Brian Boyd
Vice President, Global Facilities Management
Johnson & Johnson

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