Advancing Sterility Technology
LTX International delivers cutting-edge VHP sterilization systems, pharmaceutical isolators, and barrier solutions trusted by life science industries worldwide.
A specialized provider of sterilization and contamination control technologies for pharmaceutical, biotechnology, and healthcare industries.
LTX International, a specialized supplier of sterilization and contamination control technologies for the pharmaceutical, biotechnology, and biosafety industries, is dedicated to supplying advanced VHP sterilization systems, pharmaceutical isolators, and related containment technologies. With our superior technology and manufacturing capabilities, we ensure a contamination-free environment essential for pharmaceutical manufacturing and quality assurance.
As a specialist in sterilization and aseptic technology, LTX International protects your valuable research data from biological contamination.
Headquartered in Seoul, South Korea, we provide top-tier equipment, as well as comprehensive validation, training, and after-sales support services, to customers worldwide, including in the Asia-Pacific region.
LTX International
1013, ACE High-End Tower 1st,
5, Digital-ro 26-gil, Guro-gu,
Seoul, South Korea
Comprehensive sterilization and contamination control solutions engineered for the most demanding pharmaceutical and biotech environments.
Patented hydrogen peroxide vaporization technology is a comprehensive sterilization and contamination control solution designed for the most demanding environments in the pharmaceutical and biotechnology fields.
It is a compact, portable device ideal for small-scale sterilization tasks, research and development environments, and laboratory isolation rooms.
This product is a compact VHP sterilization system capable of sterilizing small spaces, pass boxes, isolators, etc., in pharmaceutical production sites.
This product is a high-capacity VHP sterilization system capable of sterilizing large spaces in pharmaceutical production facilities.
This is a VHP sterilization system connected to the cleanroom's HVAC system, capable of supplying hydrogen peroxide gas to each room via supply ducts.
Purpose-built VHP Chambers provide controlled sterilization environments for materials transfer, equipment decontamination, and process-specific applications requiring a dedicated sterilizable enclosure.
A pass-through unit designed for the transfer of materials between two areas of different cleanliness levels, using VHP sterilization to ensure contamination-free transfer.
A high-capacity pass-through chamber that enables the transfer of bulky materials and equipment between cleanroom zones, providing complete VHP biological decontamination capabilities.
This product is a vacuum-assisted VHP sterilization chamber that creates a vacuum inside the chamber before supplying hydrogen peroxide. This allows hydrogen peroxide vapor to penetrate deep into complex shapes, porous materials, and hard-to-reach surfaces, and enables rapid vapor removal during the aeration process.
Our isolators and RABS provide the highest level of protection for workers and products during aseptic processes, sterilization testing, and the handling of high-potency compounds, and fully comply with international regulatory standards.
Dedicated isolator for USP <71> and EP 2.6.1 sterility testing. Provides ISO 5 (Grade A) environment within the working zone, eliminating false positives and ensuring regulatory compliance.
Aseptic processing isolator for filling, compounding, and sterile manufacturing operations. Designed to meet FDA and EMA aseptic processing guidelines with robust contamination control.
Restricted Access Barrier Systems (RABS) offer an open or closed barrier solution for aseptic processing lines, combining the flexibility of an open cleanroom with enhanced contamination control.
The GLT-4000A is an automated glove integrity tester designed to detect leaks in isolator gloves quickly and reliably. Regular glove leak testing is mandated by GMP regulations and is essential for protecting both operators and products in aseptic environments.
| Model | GLT-4000A |
|---|---|
| Test Method | Pressure Decay |
| Test Pressure | 1,000 Pa (adjustable) |
| Pressure Accuracy | ± 1 Pa |
| Test Time | ≤ 60 seconds |
| Glove Size | Size 7 – 10 (all standard sizes) |
| Power Supply | Rechargeable Li-ion battery |
| Data Transfer | Bluetooth / USB |
| Display | Color touchscreen LCD |
| Alarm | Visual & audible Pass/Fail indication |
| Compliance | ISO 14644, EU GMP Annex 1, USP |
| Certification | CE Marked |
Beyond equipment supply, LTX International provides end-to-end support to ensure your systems perform to the highest standards throughout their lifecycle.
We provide comprehensive validation support including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for all our systems. Our validation packages are fully documented and compliant with FDA 21 CFR Part 11, EU GMP Annex 15, and ISO standards.
Our expert-led training programs are designed to empower your team with the knowledge and practical skills required to safely operate, maintain, and troubleshoot LTX systems. Training sessions are available on-site or remotely.
LTX International is committed to long-term customer success. Our dedicated after-sales service team provides fast, reliable support to minimize downtime and keep your operations running at peak performance.
Access our library of experimental data, validation reports, and technical studies to support your qualification and regulatory submission processes.
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Have a question about our products or services? Our team is ready to assist you. Reach out to us through any of the channels below.
1013, ACE High-End Tower 1st,
5, Digital-ro 26-gil, Guro-gu,
Seoul, South Korea
Monday – Friday: 09:00 – 18:00 KST