Pass Through Box
A complete line of material pass-throughs and transfer chambers designed for controlled and safe transfer between environments with different classification levels.
Ideal for pharmaceutical, biotechnology, and cleanroomapplications , the series includes material transfer ports and aseptic transfer chambers for sterile materials, featuring active biodecontamination systems .
These solutions comply with key regulatory requirements, including EU GMP Annex 1, cGMP, GAMP 5, and FDA 21 CFR Part 11, ensuring high standards of safety and process control.
Used in contexts of:
Pass Through Box
Available Models
The product line includes material transfer systems and cleanroom transfer chambers, available in standard and custom configurations, designed to meet specific process, installation, and material handling requirements.
The solutions include aseptic transfer chambers and systems dedicated to the transfer of sterile materials, with the option to integrate active biodecontamination systems.
Walk-in configurations are also available, designed for the transfer of larger materials.
Select the model that best suits your needs and access the corresponding technical data sheet to learn about its features, configurations, and applications.
3 modelli disponibili
Immagine prodotto non disponibile
Custom-designed Active Bio-decon Pass Through Chambers
Immagine prodotto non disponibile
Active Bio-decon Pass Through Chambers
Nessun prodotto disponibile per questa selezione.
Approach: Synergies
Beyond the Product: Design, Integration, Continuity
Hot Cells isn't just a "off-the-shelf" option. Its value lies in how the system is integrated and optimized within your specific context.
Integration
Design that is consistent with actual access points, utilities, and operational sequences. In practice:
- layout and accessibility for operators and maintenance personnel
- technical procedures and system interfaces
- Compatibility with workflows and material transfers
Customization
Configuration based on constraints and requirements, not on “standard options.” In practice:
- layout and accessibility for operators and maintenance personnel
- technical processes and system interfaces
- Compatibility with workflows and transfers
Support in the Global Context
A structured launch and operational continuity over time.
In practice:
- Controlled commissioning and handover
- Operational training and procedures
- service plan, spare parts, technical support
Services
Project Support Services
Sales Services
Solutions and expertise to support your project, from the initial analysis phase through to full operation:
-
Consulting
-
Design and Ergonomic Analysis
-
Installation and Validation
-
Training
Explore Our Sales Services
After-Sales Services
Comprehensive support even after installation, to ensure operational continuity, efficiency, and maximum performance over time:
-
Maintenance Service
-
Spare Parts Service
-
Help Desk
-
Production Support
-
Training
Reliability
Quality and Compliance Integrated into the Design
Quality and compliance are an integral part of how we work, at every stage.
- Checks and verifications throughout the various stages
- Traceability, Requirements, and Changes
Quality System
.webp?width=2000&height=1334&name=ABPTC-walkin-pass-box%20(2).webp)
Request a Technical Evaluation
Share your requirements and project specifications: we’ll provide you with initial feedback on the solution and configuration best suited to the application you’re developing.
- Application and process requirements.
- Layout, material flows, and transfer.
- Timelines and operational goals.
Other Types in the Pharmaceutical and Biotech Sectors
Is this not the type you were looking for?
If Material Passes aren't what you're looking for, check out Tema Sinergie's other solutions for the pharma and biotech industries.
QC Isolators
Sterility testing and pharmaceutical quality control isolators, designed to ensure fast processes, maximum result reliability, and compliance with cGMP regulations.
Integrity Testing Systems
Advanced devices for integrity testing of critical components of pharmaceutical isolators, such as glove ports and RTPs, designed to ensure process safety, result reliability, and full compliance with cGMP and Annex 1 regulations.
Pharmaceutical Isolators
Isolation systems for sterile and high-containment processes, designed to ensure product quality, operator safety, and regulatory compliance.
RABS
RABS systems for aseptic pharmaceutical processes, designed to ensure process protection and GMP compliance, with flexible solutions that can be integrated into both new and existing lines, including retrofitting applications.
Aseptic Filling Solutions
Automated aseptic filling and closing solutions, designed to ensure maximum sterility, process integration, and full compliance with the most stringent cGMP regulations, available for a wide range of container types.
Pass Through Box
Solutions designed to enable the aseptic transfer of materials between two separate cleanrooms while maintaining environmental isolation and minimizing the risk of contamination.