Life Science Outsourcing

Validation Testing Services

FDA-Registered Manufacturing FacilityISO 13485 Certified Quality System12 Cleanrooms Class 5–8125,000+ Sq Ft Regulated Manufacturing3 Facilities CA | NH | Costa Rica

Medical Device Validation Testing for Sterility and Compliance

Sterilization and validation testing are essential to ensuring medical device safety, regulatory compliance, and successful commercialization. Life Science Outsourcing (LSO) provides end-to-end validation testing services to support medical device manufacturers from development through commercial production.

As an FDA-registered, ISO 13485–certified contract manufacturer, LSO supports compliance with ISO 11135, ISO 17665, ISO 11737, ISO 10993, and USP standards. Our integrated testing capabilities reduce risk, simplify validation, and accelerate timelines.

Validation Testing Services

FDA-Registered

Manufacturing Facility

ISO 13485

Certified Quality System

12 Cleanrooms

Class 5–8

125,000+ Sq Ft

Regulated Manufacturing

3 Facilities

CA | NH | Costa Rica

Ready to get started?

Talk to a specialist about validation testing services.