2020 Semi-Annual Medical Device Sterilization Conferences

 October, 2020 | Arlington, VA
 December, 2020 | San Diego, CA

2020 Semi-Annual Medical Device Sterilization Conferences
 October, 2020 | Arlington, VA
 December, 2020 | San Diego, CA

Request Invite

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:

Complexity of medical product design requires a thoughtful and comprehensive approach to product sterilization, incorporating regulatory demands, a balanced approach to residual limits as well as concerns surrounding biocompatibility, in an environment where traditional methods of sterilization are currently being reconsidered. An exploration of current best practices, as well as forward thinking solutions to projected concerns will ensure medical device sterilization executives not only select the most appropriate method of sterilization but also meet evolving consumer and regulatory demands.

Core Topics to be Addressed:

  • Current research & perspectives on EtO sterilization
  • Exploration of new modalities of device sterilization
  • Alignment of sterilization with FDA + ISO regulation
  • Use of parametric release to support device sterilization
  • Impact of EU MDR & EU residuals on sterilization of devices

Program Highlights:

  • Varied perspectives from industry & regulators
  • Facility perspectives on device reprocessing
  • Interactive by nature, focused on problem solving

Core Topics to be Addressed:

  • Current research & perspectives on EtO sterilization
  • Exploration of new modalities of device sterilization
  • Alignment of sterilization with FDA + ISO regulation
  • Use of parametric release to support device sterilization
  • Impact of EU MDR & EU residuals on sterilization of devices

Request Invite

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

Audience

75 Attendees

All attendees come directly from medical device companies

Distinguished Presenters

Speaker recruitment in progress

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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