Operator protection
Systems can be configured to reduce exposure during filter replacement, handling, access or transfer operations.
Products · Containment Systems
Containment Systems
Barrier, sealing and containment equipment for pharmaceutical, biotech and controlled cleanroom environments.
Overview
Containment equipment designed around controlled environments.
Montcasyer designs and manufactures containment systems for pharmaceutical, biotech and cleanroom facilities where separation, sealing performance and controlled access are critical.
Equipment can be supplied as individual units or integrated into wider cleanroom, process or HVAC systems depending on the facility layout and containment requirements.
Controlled separation
Equipment supports physical separation between clean, contained or classified areas through barriers, valves and airtight interfaces.
Facility integration
Units are designed according to room pressure strategy, installation details, cleaning requirements and maintenance access.
Containment equipment
BIBO Systems
Bag-in bag-out systems are designed for safe filter replacement in areas where containment integrity and operator protection must be maintained during maintenance operations.
Filter replacement
BIBO housings allow filters to be removed and replaced through a bagging system, reducing direct exposure to contaminated or hazardous material.
Containment integrity
Housing geometry, sealing surfaces, clamping systems and access points are defined to support controlled maintenance procedures.
Typical configuration
- Safe filter change systems
- HEPA or process filtration housings
- Bag-in bag-out access ports
- Stainless steel construction
- Cleanroom or technical area installation
- Project-specific dimensions and connections
Containment equipment
Bioseal Valves
Bioseal valves provide controlled sealing between process equipment, cleanroom boundaries and containment interfaces where reliable closure and hygienic construction are required.
Sealing function
Bioseal valves are used to maintain separation between controlled areas, process volumes or transfer points while supporting cleaning and inspection.
Clean interface
Design focuses on sealing reliability, smooth contact surfaces, material compatibility and integration with stainless steel systems.
Typical configuration
- Containment and sterile interfaces
- Manual or actuated operation
- Stainless steel construction
- Process or room integration
- Custom dimensions available
- Documentation according to project scope
Containment equipment
Airtight Doors
Airtight doors are engineered for cleanrooms and containment areas where pressure control, sealing performance and controlled access are part of the facility design.
Room separation
Doors support controlled separation between rooms or technical areas, helping maintain pressure cascades and cleanroom boundaries.
Mechanical execution
Frames, panels, gaskets, hinges and locking systems are manufactured in stainless steel in accordance with applicable material standards and selected according to installation requirements and operational use
Typical configuration
- Cleanroom access doors (Available in manual or automatic operation)
- Containment area doors
- Airtight gasket systems
- Stainless steel or compatible finishes
- Single or double-leaf execution
- Custom dimensions and installation details
Containment equipment
Isolators
Isolators provide a physical barrier between the operator, product and surrounding environment during pharmaceutical and biotech operations requiring controlled handling.
Barrier protection
Isolator design supports controlled manipulation through sealed interfaces, reducing direct contact between operators and the process environment.
Process adaptation
Chambers, transfer systems, glove ports, access doors and utilities can be configured according to the operation and containment strategy.
Typical configuration
- Operator and product protection
- Glove port operation
- Transfer and access systems
- Stainless steel chamber construction
- Integrated filtration or ventilation options
- Project-specific layout and documentation
Technical scope
Typical configuration parameters
Equipment type BIBO systems, bioseal valves, airtight doors and isolators
Material Stainless steel construction, project-specific finishes available
Application Cleanrooms, containment areas, technical rooms and process interfaces
Execution Standalone equipment or integrated facility component
Sealing Defined according to containment, pressure and cleanroom requirements
Access Manual, assisted or project-specific access configurations
Integration Room envelope, HVAC, filtration, process or transfer systems
Documentation Drawings, technical files and certificates according to scope
Support Engineering support, installation coordination and commissioning assistance
Documentation
Technical documentation for controlled environments.
Containment equipment can be supplied with project-specific documentation supporting installation, inspection, maintenance and regulated facility requirements.
- Technical drawings
- Material certificates
- Installation details
- Surface finish documentation
- Operating and maintenance manuals
- Inspection records
- FAT and SAT support
- Project-specific technical files
Technical enquiry
Discuss a containment system requirement.
For containment equipment, cleanroom integration or project-specific technical requirements, contact Montcasyer’s engineering team