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

Reserve Your Space

Attendees at the Quality Manufacturing Conference will be looking to not only learn about best practices in the industry, they also want to find out what the latest and greatest products in lifecycle and data management, pharmaceutical manufacturing, and more. Highlight new products or build brand awareness to YOUR target audience. Put your company in front of the industry’s top decision makers and influencers by submitting your exhibit contract today. Don’t delay, spaces are selling quickly!

Exhibit Application Exhibit Hall Floor Plan

Exhibit Packages

*Early Bird Deadline: 13 March 2017

Standard Package $1,750* | $1,950

  • One 6’x2’ skirted table with chair and one-line identification sign
  • Two complimentary exhibitor badges (fee applies for an additional badge)
  • Admission to education sessions for up to two exhibiting personnel (space-available basis)
  • Company listing on the ISPE mobile app and in the printed exhibitor directory portion of the event guide (deadlines apply)
  • Complimentary listing in ISPE’s online searchable exhibitor directory
  • Two complimentary guest passes for exhibit hall admission
  • Welcome reception, lunch, and networking breaks held in exhibit hall

Premium Package $2,050*| $2,250

All items listed for Standard package, plus:

  • Priority choice of table selection (based on registration date; subject to availability)
  • Enhanced listing in exhibitor directory featuring:
    • Company logo and outline border
    • Link to company website in online version

Premium Spotlight Package $2,250* | $2,450

All items listed for Premium package, plus:

  • 5-minute (maximum) unmanned, self-running presentation with audio to play on plasma screen during networking breaks

10’ x 10’ Booth Package $2,850* | $3,100

All items listed for Standard and Premium packages, plus:

  • Pipe & drape – 7’ high across back & 3’ side walls
  • One additional complimentary exhibitor badge

Booth Spotlight Package $3,100* | $3,350

All items listed for 10x10 booth package, plus:

  • 5-minute (maximum) unmanned, self-running presentation with audio to play on plasma screen during networking breaks

 Additional Questions? Please contact:

Alisa Pachella, Account Manager, Sales
Telephone: +1-813-739-2274
Email: apachella@ispe.org


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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