In part one of Eurofins’ Ophthalmic Webinar series, experts Rick Camp and Katie Grayson share their approaches for ensuring ophthalmic medical device compliance for intraocular lenses, surgical injectors, contact lenses, and related materials.
In this session you will learn how to assess and mitigate risks associated with extractables and leachables testing, raw materials testing, packaging and distribution testing, and human factors engineering for ophthalmic devices.
This webinar will be the first of a two-part series. All registrants will receive an invite to join Eurofins for part two in September 2025.
During this webinar you will learn:
Presenters:
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Rick Camp General Manager Eurofins Medical Device Services |
As General Manager of Eurofins Medical Device Services in Cary, NC and Jacksonville, FL, Mr. Camp oversees laboratory operations across two Eurofins’ facilities. With more than 30 years of experience in Analytical Chemistry & Laboratory Management, and over 20 years of experience managing GMP labs, Mr. Camp and his team bring extensive experience in Ophthalmic Formulation Development & Optimization and Clinical Trial Material Manufacturing to the Eurofins’ network of laboratories.
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Katie Grayson General Manager Eurofins Medical Device Services |
As General Manager of Eurofins Medical Device Services in St. Louis, MO, Ms. Grayson oversees the day-to-day operations of the laboratory and focuses on chemical characterization, extractables/leachables testing, with a specialty in solving formidable analytical challenges.
Ms. Grayson has more than 25 years of experience in bio/pharmaceutical and medical device analysis, contract laboratory testing, and 15+ years of laboratory sales and operations management, which has played a pivotal role in the laboratory’s growth. Ms. Grayson is an alumna of the Goldman Sachs 10,000 Small Business Program. She holds a bachelor’s degree in chemistry.
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In part one of Eurofins’ Ophthalmic Webinar series, experts Rick Camp and Katie Grayson share their approaches for ensuring ophthalmic medical device compliance for intraocular lenses, surgical injectors, contact lenses, and related materials.
In this session you will learn how to assess and mitigate risks associated with extractables and leachables testing, raw materials testing, packaging and distribution testing, and human factors engineering for ophthalmic devices.
This webinar will be the first of a two-part series. All registrants will receive an invite to join Eurofins for part two in September 2025.
During this webinar you will learn:
Presenter:
![]() |
Rick Camp General Manager Eurofins Medical Device Services |
![]() |
Katie Grayson General Manager Eurofins Medical Device Services |