
About Us
Andersen Scientific is an extension of your R&D team, bringing specialized knowledge and environmentally responsible sterilization solutions to medical device pioneers.
Built by Sterilization Professionals
ANSCI was founded to serve clients who need technical depth and responsiveness, not just capacity. Our team brings decades of hands-on EO sterilization, validation, and regulatory experienceâand we stay personally involved in every project. We take pride in:
- communicationClear communication
- thumbs_up_downConservative, defensible decisions
- check_circleDoing things onceâand doing them right

What Sets Us Apart
Facts that define our commitment to medical device excellence.
Direct Engineer Access
Work directly with sterilization engineersânot account managers or ticketing systems.
Flexible Chamber Design
Chambers configured for small to medium load volumes, optimized for precisionânot throughput.
EO Validation Expertise
Deep expertise in EO validation strategy and executionânot just running cycles.
Audit-Ready Documentation
Practical, defensible documentation aligned with ISO standards and FDA expectations.
FDA Sterilization Master File
Sterilization Master File access on record with the FDA to support your regulatory submissions.
Organizations that need technical partnershipânot just processing capacity.
While our core focus is supporting small and mid-sized organizations, we are also engaged by large, global manufacturers for specialized projects that require a high level of technical expertise and direct engineering involvement.
If your project needs careful thoughtânot just capacityâweâre the right partner.
Medical Device Startups
Early-stage and emerging companies navigating first validations and regulatory submissions.
Small to Mid-Sized Manufacturers
Device companies seeking flexible EO sterilization aligned with evolving production needs.
Pharma & Drug Development
Pharmaceutical and drug development organizations requiring specialized sterilization support.
Universities & Research Institutions
Academic and translational research programs working on novel devices and packaging systems.
Hospitals & Clinical Programs
Clinical research groups and healthcare systems requiring controlled EO sterilization support.
Life-Science Laboratories
Tissue culture and laboratory environments requiring validation rigor and documentation clarity.
Requalification & Equivalence Projects
Organizations requiring requalification, adoption, or equivalence strategy support.
How We Work
A deliberate, engineering-driven process from first discussion through regulatory support.
Understand Your Device and Goals
We begin with how your device is used, packaged, and manufacturedâ so the sterilization approach reflects real-world use.
Design a Sensible Strategy
Validation methods are selected based on risk, material compatibility, and regulatory pathwayânot habit.
Execute with Control & Documentation
Data integrity, traceability, and clear documentation are built into every stage of execution.
Support Beyond the Cycle
We remain available to help you explain and defend the workâ not just complete it.
Transparency
Youâll always know
Registered and audited for medical device work
Andersen Scientific maintains the highest regulatory and environmental standards.
- ISO 13485 Certified & Registered with the FDA (Est. No. 1064858)
- FDA Innovation Challenge 2 Winner
- Small Business Environmental Stewardship Award recipient
- NC permit exemption for exceptionally low emissions

The Team
Experienced professionals committed to your device's success.

A.E. Ted May
President
A.E. Ted May
President

Daryl Woodman
GENERAL MANAGER

Daryl Woodman
GENERAL MANAGER

Benjamin Watts
STERILIZATION MANAGER

Benjamin Watts
STERILIZATION MANAGER

Conor Russell
VALIDATION ENGINEER

Conor Russell
VALIDATION ENGINEER

Daniel Lim
REGULATORY AFFAIRS
Daniel Lim
REGULATORY AFFAIRS

Rushon Carey
Technical Lead

Rushon Carey
Technical Lead