Event Type: Industry Conference | Date: September 24, 2018- September 25, 2018 | Location: Millennium Minneapolis Hotel - Minneapolis, MN

We’re presenting at the Q1 Productions 5th Annual Medical Device Sterilization Conference at the Millennium Minneapolis Hotel in Minneapolis, MN

“The Q1 Productions 5th Annual Medical Device Sterilization Conference will bring together industry leaders, regulatory bodies and solution providers to discuss topics of key importance and timely concern. Via a mix of formats including panel discussions, exchange groups, workshops and traditional presentations, attendees have the opportunity to take away actionable content through engaging sessions and the sharing of best practices. Further and as always, the event will offer a unique networking platform for delegates to connect with a multitude of key experts in the field.”

 

Join Carrie Clark, Director of Gas Technology, STERIS AST in a panel discussion on:

• Increasing sterilization demands impact on contract sterilizer capacity
• Contract sterilizer capacity level assessment methods
• Manufacturer’s need for contractor’s capacity assurance
• Contractor’s need for manufacturer’s supply assurance
• Opportunities in building win-win partnerships for both parties

 

Attend “Opportunities in EO Residuals Decrease via Optimized Control of Overkill Validation,” with Ken Gordon, Sr. Scientist, STERIS AST as he presents:

• Avoiding “over-overkill” validation methods
• Defining where to place the BI for effective testing
• Validating to a more reasonable, yet safe level
• Overall sterility with minimized EO residuals

 

Stop by Q1 Productions 5th Annual Medical Device Sterilization Conference to speak to one of our STERIS AST experts on product development, laboratory testing/validation and routine sterilization.

Register