Certifications
Discover Life Science Outsourcing's certifications as a top-tier medical device assembly Contract Manufacturing Organization, showcasing our FDA-registered and ISO 13485-certified commitment to quality and excellence.
Life Science Outsourcing has an unwavering commitment to quality and evolving industry requirements.
As an FDA-registered and ISO 13485-certified contract manufacturing organization, we excel in medical device assembly, packaging, sterilization, and diagnostics (wet reagent packaging) for the life science sector. Our end-to-end services, coupled with extensive regulatory knowledge, ensure streamlined processes for accelerated go-to-market launches. Explore our range of certifications that underline our continued commitment to superior quality management and risk mitigation in the medical device assembly field.
Life Science Outsourcing’s Certifications
- International Standard ISO 13485:2016 (Brea, CA)
- International Standard ISO 13485:2016 (Somersworth, NH)
- FDA CDRH Registration: Contract Manufacturer, Contract Sterilizer
- FDA CDRH Registration: Contract Manufacturer (Somersworth, NH)
- State of California: Device Manufacturing License
- International Standard ISO 17665-1:2006 Moist Heat Sterilization
- International Standard ISO 11135:2014 Contract Ethylene Oxide Sterilization and Validation Services
- CDER Drug Sterilization Registration
- State of California: Drug Manufacturing License
- Japan Minister of Health: Medical Device Manufacturer, Sterile and Non Sterile Devices
- ISTA Certified Package Testing Laboratory
About LSO
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