Sterilization Service

Supply of gamma/EOG sterilization-compatible consumables and sterilization service

Sterilization Service

Seoul Semitech provides end-to-end support—from sterilization process planning to specification adjustment and history management—for pharmaceutical and bio-industry consumables that require gamma or EO Gas sterilization. We can respond with the appropriate sterilization method and manage proper specifications for sterilizable product lines such as gloves, goggles, masks, and wipers, and our strength lies in customizing post-sterilization packaging specifications, storage conditions, and shelf life to each client's quality standards. All sterilized items can be verified for sterilization history and issued a CoA/sterilization certificate per product before shipment.

Available Sterilization Services

Gamma Sterilization

Complete penetrating sterilization using gamma rays

Gamma rays completely sterilize even packaged products, and being non-toxic, they are ready for immediate use

1Strong penetration power
2Can sterilize in fully packaged state
3Ready for immediate shipment
4No harmful residual gas
5Excellent cost efficiency for large lots
6Compliant with international standards

EOG Sterilization

Low-temperature penetrating EO Gas sterilization

저온 공정과 우수한 침투력으로 포장된 미세 구조 의료기기까지 완벽하게 멸균합니다.

1Low-temperature sterilization process
2Excellent gas penetration
3Can sterilize in final packaged state
4Optimal for heat/moisture-sensitive products
5Easy penetration into complex structures and fine pores
6Cost efficiency secured through large batch processing
Sterilization Process
STEP 1
Reception & Package Inspection
STEP 2
Pre-treatment (Temperature/Humidity Setting)
STEP 3
EO Injection OR Gamma Irradiation
STEP 4
Aeration or Cooldown
STEP 5
Quality Inspection (BI/CI)
STEP 6
COA & Validation Report Issuance
STEP 7
Shipment Approval & Delivery

※ Temperature, gas concentration, irradiation dose, and other data are automatically recorded throughout the process

Core Capabilities
01

Validation-BasedSterilization Management

IQ/OQ/PQ documentation andsterility & residual test data provided

Compliant with international standards / quantitative validation documents secured / AUDIT-ready

02

Sterilization Certificate &Cycle History Provided

COA, sterilization cycle reports, andother official documents issued

Per-product sterilization history tracking / documentation ready for client submission

03

Regular Sterilization Operations &Regulatory Response Experience

From initial consultingto regular sterilization, fully supported

Meets pharmaceutical/bio standards / proven domestic GMP track record