Description
The North American Biocompatibility Summit (NABS) is a limited-seating event that provides industry insights and expertise sharing on the biocompatibility of medical devices. This year, sessions will include the latest regulatory updates, biological evaluation strategies and best practices that lead to successful biocompatibility programs.
Led by the medical device industry’s foremost biological safety experts, speakers will address:
- Regulatory strategies and how they relate to ISO 10993
- New and innovative biocompatibility methods and technologies
- The relationship between material/chemical characterization and biocompatibility testing
- Toxicology and risk management
- Industry case studies
REGISTRATION PRICING
- Early-Bird (ends August 3): $275.00
- Regular: $475.00
Call for Abstracts
The dynamic landscape of biocompatibility presents unique challenges across different regions. The upcoming Summit is the perfect platform to address these issues, share best practices, and explore advocacy efforts aimed at easing regulatory pressures on manufacturers.
We are seeking submissions from Toxicologists, Scientists, and industry leaders specializing in biocompatibility. Following last year’s success, the NABS Scientific Board is eager to maintain a focus on global hurdles of chemical characterization and biocompatibility for the 2025 agenda. (All accepted abstracts/speakers will receive a complimentary pass to this limited seating event.)
To submit your abstract, please click here. Abstracts submitted without a detailed description and objectives will not be considered. The deadline for submissions is June 8, 2025.
For inquiries about abstract submission, please contact Sheri Krajewski at: sbibins@namsa.com.
For regular updates, please visit www.nabiocompsummit.com anytime.
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