Litek Pharma offers a comprehensive range of isolators for aseptic and aseptic-toxic processing, designed to meet the most demanding requirements of pharmaceutical and biotechnology production.

Each isolator is modular in design and can be precisely configured to suit the specific needs of every project — from sterility testing units and small-scale filling systems to fully customized large-scale production isolators.

With proven engineering expertise and strict compliance with international standards, Litek Pharma ensures every isolator delivers maximum contamination control, operator safety, and process reliability across all applications.

Litek Pharma’s Small-Scale Fill & Finish Isolator is a customizable aseptic enclosure designed for various filling operations in pharmaceutical and biotech applications.

It supports multiple filling machines for vials, syringes, and bottles, handling both liquid and powder products with precision and sterility.

Developed to prevent external contamination, it ensures product integrity and aseptic conditions. For containment processes, the isolator can be configured to provide both aseptic operation and operator safety, fully in line with GMP standards.

Litek Pharma’s DWI Isolator is a double-walled, high-performance system designed to ensure maximum protection during aseptic and aseptic-toxic filling processes. Ideal for customised filling lines and freeze-drying systems, it maintains a Grade A (ISO 5) internal environment with precise control over pressure, temperature, humidity, and particulates.

Engineered for installation in Grade D cleanrooms under EU-GMP standards, the isolator offers seamless integration with fillers or freeze dryers and can be configured with multiple airlocks for flexible material and personnel transfer.

In advanced therapy production, maintaining a safe and aseptic environment is essential. Litek Pharma’s ATMP Isolator provides a controlled, sterile enclosure that enables sensitive processes to be carried out with the highest level of product and operator protection.

Compared to traditional cleanrooms or laminar flow booths, Litek’s isolators offer superior contamination control and process sterility, fully integrated within a compact modular system.

Each isolator can be configured to house critical laboratory equipment such as centrifuges, incubators, refrigerators, gene modification devices, and systems for both upstream and downstream cell processing — ensuring flexibility and compliance for advanced therapy manufacturing.

Litek Pharma’s Containment Isolators are designed to create a safe and controlled environment for handling high-potent or highly active pharmaceutical ingredients (HAPI), ensuring complete operator protection during toxic or hazardous processes.

Engineered and validated up to OEB5 (OEL ≤ 50 ng/m³), these isolators provide the highest level of containment performance while maintaining process efficiency and ergonomic operation.

Built on a modular design concept, Litek isolators can be customised to suit specific process requirements, allowing seamless integration from concept development to final qualification.

Sterility testing is an essential step in releasing sterile drug batches, ensuring that the final product is free from microbial contamination. To guarantee accurate results and avoid false positives, Litek Pharma’s Sterility Test Isolators provide a controlled aseptic environment that enables reliable and contamination-free testing.

The system’s modular design allows full customisation based on testing volume and workflow requirements — including varied isolator sizes, Pass-Through SAS, and material or waste transfer modules — delivering flexibility, safety, and compliance for every laboratory setup.

Litek Pharma’s Glove Tester is a self-contained, wireless device designed to verify glove integrity with precision and ease. Connected via Wi-Fi to the isolator’s control system, it enables seamless monitoring and data recording in compliance with GAMP5 standards.

Equipped with an integrated pump, fan, battery, and instrumentation, the unit performs reliable leak tests and automatically stores the results for full traceability. Its intuitive user interface ensures simple operation and efficient glove testing for routine use.

Litek Pharma’s Rapid Transfer Port (RTP) Tester is a wireless integrity testing device designed to verify the airtightness of material transfer systems in aseptic and containment environments. It ensures that no air leaks or contamination occur during transfer, maintaining product quality and operator safety in pharmaceutical and biotechnology applications.

Compatible with Alpha rapid transfer ports and Beta transfer containers, this cable-free solution delivers accurate, repeatable, and traceable leak detection, guaranteeing full process integrity in aseptic and toxic handling operations.