Process Isolators
Are you ready for OEB 7 ?
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Toxic - Sterile - Sterile/Toxic Process
In pharmaceutical manufacturing, effective containment is essential to protect operators and prevent cross-contamination.
Dec offers a comprehensive range of isolator technologies for safe, flexible powder handling and seamless integration into diverse production environments.
We deliver turnkey containment solutions for potent and aseptic materials, including custom-built systems that meet evolving industry demands while adhering to current health, safety, and regulatory standards.
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Nanogram-level containment
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SMEPAC-validated performance
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Process-integrated and modular designs
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Uncompromised operator and product protection
Whether you're scaling up or refining your process, Dec delivers containment you can trust.
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BioDec® Advanced Decontamination
Aerosolized Hâ‚‚Oâ‚‚: A New Approach to an Old Molecule
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BioDec® introduces a new generation of rapid, reliable, and fully integrated H2O2 decontamination method for isolators. Powered by its dry fog generation system and Dec’s catalytic panel technology, BioDec® delivers highly efficient bio decontamination cycles.
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Aerosolized Hâ‚‚Oâ‚‚ uses pressurized nozzles to create a fine, uniform dry-fog that fills the chamber rapidly and reliably. This approach delivers faster cycles, better coverage, and far greater tolerance to environmental conditions. With no hotplate or vaporizer, the hardware is simpler and more robust, and cycle development becomes predictable and scalable across sites. When paired with catalytic aeration, chambers return to operation dramatically faster.
The result is a decontamination process that’s faster, cleaner, more consistent, and easier to validate - built for the demands of modern pharmaceutical manufacturing.
Key Benefits
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Validated spore 6-log reduction
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Much shorter cycles
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Uniform distribution
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Formula-based scalability
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Simpler space-saving hardware
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Catalytic residual breakdown
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Less energy and Hâ‚‚Oâ‚‚ consumption compared to VPH
Phase 1 - Preconditioning
Humidity is lowered and the system is primed with Hâ‚‚Oâ‚‚ to create ideal starting conditions.
Phase 2 - Conditioning
A controlled amount of Hâ‚‚Oâ‚‚ is nebulized into the isolator and CG void to reach the target concentration.
Phase 3 - Decontamination
The chamber holds a stable Hâ‚‚Oâ‚‚ level for the required exposure time to ensure effective microbial kill.
Phase 4 - Aeration
Fresh HEPA‑filtered air and catalytic panels rapidly remove residual H₂O₂ to below 1 ppm, with all exhaust safely filtered before returning to the room.
Glove Integrity Testing
DGT Ex
Dec provides fully automated, single and multi-port glove testers which are instantly ready to verify the integrity of your gloves.
These simple to use mobile devices are compatible with all glove types (CSM, EPDM, etc.).
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The cGMP compliant hygienic design of the version which includes air supply allows for easy cleaning and sterilization procedures.
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Product sheet (multi-port system, excluding air supply)
DGT Pro (wireless)
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High-performance, flexible, and economical glove integrity testing system:
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Long‑range wireless communication without cable constraints
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RFID‑based glove identification and complete test history
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Adaptable to various glove port designs and dimensions
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Mobile docking and recharging station engineered to store and recharge 10 glove testers
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Detection of micro‑defects ≥100 μm
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Centralized data traceability with comprehensive audit trails
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Full compliance with GMP Annex 1, ISO 14644‑7 Annex 5, 21 CFR Part 11, and EU Annex 11
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