2019 Semi-Annual Medical Device Sterilization Conference

October 29-30, 2019 | Arlington, VA
December 10-11, 2019 | San Diego, CA

2019 Semi-Annual Medical Device Sterilization Conference
October 29-30, 2019 | Arlington, VA
December 10-11, 2019 | San Diego, CA

Download Agenda - Arlington

Download Overview - San Diego

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

“I thought the conference was excellent!  Having a conference tailored to one discipline made each panel and contact relevant.”

Director, Compliance & Legal Affairs
Orexigen

“Great insight to hear payer perspective in contracting and account management and the changing healthcare landscape.”

Channel Liaison
Biogen

“It was definitely an excellent well-rounded opportunity to meet new people, get new ideas, and get an in-depth education on what’s to come with the FDA collaborations.”

Quality Engineer
Centurion Medical Products

“It was very well organized event and high quality, the fact to have an IVD track was also interesting. Thanks, I will recommend the Q1 event!”

Regulatory Affairs – EMEA Regional Head
BIOMERIEUX

“The organization and support staff were fantastic! I’m looking forward to next year.”

Global Business Project Lead
Genentech

About the Conference:

Throughout the medical device industry, executives responsible for product sterilization are continuously evaluating processes and the technology used to ensure robust sterilization, validation and bio-compatibility. As devices become increasingly complex and integrate new technology, combination products and systems, ensuring the appropriate sterilization method is selected and conducting robust validation of the selected method is essential.

Core Topics to be Addressed:

  • Practical Methods for Optimizing Sterilization Cycles
  • Enhanced Biocompatibility Testing & Chemical Analysis
  • Impact of International Residuals Restrictions on Devices
  • Decreasing EO Residuals through Enhanced Validation
  • Continuous Optimization of Sterilization Validation Practices
  • Role of Sterilization in the Increasing Reusables Market

Program Highlights:

  • 20+ Industry Presenters Sharing In-Depth Case Studies
  • Contract Sterilizers Showcasing New Technologies
  • Small Group Discussions to Support Peer-to-Peer Learning

Core Topics to be Addressed:

  • Practical Methods for Optimizing Sterilization Cycles
  • Enhanced Biocompatibility Testing & Chemical Analysis
  • Impact of International Residuals Restrictions on Devices
  • Decreasing EO Residuals through Enhanced Validation
  • Continuous Optimization of Sterilization Validation Practices
  • Role of Sterilization in the Increasing Reusables Market

Download Agenda – Arlington

Download Overview – San Diego

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

Audience

75 Attendees

All attendees come directly from medical device companies

Distinguished Presenters

17 Speakers

Networking

Networking time is built into the agenda to allow industry peers to connect and exchange ideas

Open Dialogue and Group Share

Each presentation is followed by 10-15 minutes of open dialogue for questions and exchange of best practices

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