Integrated Containment Solutions Across Critical Pharma Processes
Our isolator portfolio is engineered to address diverse containment requirements across pharmaceutical manufacturing—from material handling and processing to testing and transfer. Each system is designed to ensure operator safety, product integrity, and regulatory compliance while seamlessly integrating into existing production workflows.
Enables in-process quality checks within a contained environment, ensuring compliance without exposing operators or materials.
Designed to contain granulation processes, preventing dust escape while maintaining process consistency and operator safety.
Ensures safe sampling and precise dispensing of powders and APIs under controlled, high-containment conditions.
Adaptable containment systems using flexible materials for cost-effective and process-specific applications.
Maintains a sterile, contamination-free internal environment for aseptic or sensitive processes.
Provides containment for tablet compression and capsule filling operations involving potent compounds.
Facilitates safe material transfer between systems using RTPs and other containment technologies.
Ensures the reliability and leak-tight performance of isolator gloves through validated testing systems.
Applications
- High-potency API (HPAPI) handling
- Granulation and powder processing
- Tablet compression and capsule filling
- In-process quality control (IPQC)
- Aseptic and sterile operations
- Material sampling and dispensing
- Safe material transfer between equipment
- Research, development, and pilot-scale operations
Advantages
- High-level operator and environmental protection
- Compliance with GMP and global containment standards
- Prevention of cross-contamination
- Process-specific and scalable configurations
- Improved workflow efficiency and reduced handling risks
- Integration with existing manufacturing systems
- Ergonomic and user-centric design
- Reliable containment performance across applications