GMP Class 2 containment enclosure designed for the most challenging containment levels during manipulations of High Potent Active Pharmaceutical Ingredients (HPAPI) for analysis/quality control activities.

The Dispensing Isolator is a GMP Class 2 containment enclosure designed for the most challenging containment levels during manipulations of potentially hazardous compounds for production activities. The isolator system is equipped with a turbulent air flow system, and constantly guarantees a negativ

The High Containment Isolator System (HC-IS) is a GMP Class 2 modular HPAPI containment enclosure designed for the most challenging containment levels during manipulations of potentially hazardous compounds for Research & Development, Production and QC. High Containment Isolator System (HC-IS) can

The Streamline® Containment Isolator Class III (SCI Class III) configuration solely operates in a negative pressure, with its on-board fan providing -37 Pa to -125 Pa (max) in the process chamber and -25 Pa to -75 Pa (max) in the pass-through chamber. "To comply fully with biosafety standards, the

There is a challenge in today’s advanced therapy environment, which is to get your preparations done in a safe environment. At LITEK PHARMA, we have prepared various solutions to enable these production processes to be carried out in a safe aseptic environment, inside the isolator. Compared to tradi

High quality manufacturing ISO 9001:2008 Leak test according to ISO 10648-2, Class 1 Stainless steel 1.4301 (AISI 304) Different sizes and shapes for 2, 3, 4 and more gloves Differently polished surfaces Double-sided versions All edges with a radius of 10 mm (easy clean) Sloped floor with drain (eas

Laminar isolators are designed to create a clean and sterile environment and to protect the product being processed or the operator. Cleanliness class: A Tightness class 3: according to ISO 10648-2. Laminar flow: 0.45 m/s ±20% (864–1533 h⁻¹) depending on the chamber volume. Construction material: sh

Suitable for manufacturers of active pharmaceutical ingredients (API category OEB-6) and oral solid dosage forms (OSD). Ensures safety for both the production team and the product. Cleanliness class: C Tightness class 3: according to ISO 10648-2. Turbulent flow: 5–40 exchanges/hour. Construction mat

The Aseptic Sampling Isolator is a custom-designed cGMP Class A/ISO 5 isolator system specifically designed for handling large containers/bags and sampling sterile powders (API).

The Aseptic Transfer Isolator is a custom-designed cGMP Class A/ISO 5 isolator system specifically designed for pharmaceautical companies which require a low rH% aseptic environment for semi-automatic transfer of liquid substances.

The Aseptic Isolator, AP-IS Series, is a cGMP Class A/ISO 5 isolator system specifically designed for R&D, batch scale pharmaceutical production and pharmacies.

The GloveFAST Cyto Pharma isolator complies with the following standards and certifications: - **DIN 12980:2017-05**: Specifies requirements for isolators used in pharmaceutical applications. - **DIN EN ISO 14644-7**: Pertains to cleanrooms and associated controlled environments, focusing on isola

Connection at your fingertips with our revolutionary Easyglide™ system in our Beta Container. Our range of aseptic transfer containers, the ABC Transfer® Beta Container, enables simple and secure transfers, thanks to our innovative Easyglide™ system. Our containers are compatible with other brands.

ABC Transfer® ULTRA™ is the first aseptic transfer system specifically designed for the sterile transfer of components via ported bags, without the need for glove ports. It combines State-of-the-Art yet simple technologies: the ABC Transfer® gloveless alpha port, the ABC Transfer® ULTRA™ Betacleanba

The complete ABC Transfer® System (RTP) is designed to power up rapid transfers in pharmaceutical filling lines.

High quality manufacturing ISO 9001:2008 Leak test according to ISO 10648-2, Class 1 Stainless steel 1.4301 (AISI 304) Different sizes and shapes for 2, 3, 4 and more gloves Differently polished surfaces Double-sided versions All edges with a radius of 10 mm (easy clean) Sloped floor with drain (eas

High quality manufacturing ISO 9001:2008 Leak test according to ISO 10648-2, Class 1 PMMA, PE (white), PETG Different sizes for 2, 3 and 4 gloves Double-sided versions Front window easy to disassemble Leveling feet and solid base stand with castors

Complete inert gas system O2 and H2O < 1ppm

Complete inert gas system O2 and H2O < 1ppm

Inert Purge box, designed for either positive or negative pressure environments, provide exceptional protection for products and processes from oxygen and moisture. These gloveboxes utilized across a wide array of applications and industries, including powder handling, packaging, climatic chambers,

I-Lab Glovebox System: Your Ultimate Solution for Inert Research Applications Experience unparalleled control over your research environment with the I-Lab Glovebox System, engineered to maintain oxygen and moisture levels below 1ppm. Perfectly suited for a wide array of applications requiring stri

PureLab HE represents Inert’s flagship glovebox product line, engineered and manufactured in the USA using the highest quality materials and craftsmanship. Designed for maximum purity and performance, PureLab HE is ideal for applications requiring stringent atmospheric control. Built on a modular p

Pass Through Chambers for aseptic transfer of materials in the cleanroom Active Bio-Decon Pass Through Chambers can be used for multiple applications, such as aseptic transfer of materials into cleanrooms or decontamination of equipment from BSL-1 through 4 organisms prior to extraction from the fa

Walk-In dimensions Pass Through Chambers for aseptic transfer of materials in the cleanroom With Active Bio-decon Walk-in Pass Through Chambers, the materials are sterilized in the Pass Through Chamber by means of an integrated Bio-decontamination system. The integrated ventilation system of the c

The CC-IS is a Cell Culture Isolator cGMP Class A/ISO 5 system specifically designed to provide the users with a cell culture environment which is safer than environments on traditional biosafety cabinets, clean booths or standard cleanrooms, by eliminating any risk from human contamination of cell