GMP Validated Temperature Storage
Receive, Store and Ship: Sentry's GMP Warehouse Agility Enhances Your Supply Chain
As guardians of temperature-sensitive products, Sentry maintains GMP validated temperature storage as a core competency. Sentry offers the following environments for clinical trial material storage, drug storage, vaccine storage and medical device storage:
- Ambient: +15°C to +30°C
- Controlled Room Temperature: +20°C to +25°C
- Refrigerated: +2°C to +8°C
- Frozen: -15°C to -25°C
- Low-Temp Frozen: -35°C to -45°C
- Custom Frozen: -40°C to -60°C
- Custom Ultra-Low: -60°C to -80°C
- Custom Ultra-Low: -65°C to -85°C
- Ultra-Low: -70°C to -90°C
- Vapor Phase Liquid Nitrogen: <-135°C
- Custom Temperature Solutions: 0°C to <-135°C
Sentry’s expertise, quality program, and validated processes present an opportunity to meet any GMP storage need. Validated IT systems, infrastructure and processes can accommodate ICH recommended drug storage ranges while allowing virtually any customized storage environment for the unique and stringent requirements of biological products.
Sentry maintains control over product classifications and locations within its GMP warehouse. This sophisticated inventory management capability supports pharmaceutical packaging, returns, quarantine, controlled substances and even enhanced security for high-risk products. Sentry’s guardianship is evident in the systems implemented and the processes utilized to mitigate risks that may adversely impact product safety, identity, strength, purity and quality (SISPQ).
- Validated temperature monitoring system for each drug storage environment
- Validated GMP warehouse management system
- Redundancy of critical systems to ensure business continuity and control
- Infrastructure for rapid implementation or expansion