Drug-Storage and Distribution Services
'Your Trusted Partner in Pharmaceutical Storage.'
At Quantime, we ensure that all Investigational Medicinal Products (IMPs) are stored in full compliance with global regulatory standards and maintained under precise temperature conditions—safeguarding product integrity at every stage.
Beyond compliance, we proactively support our clients with demand planning and site-level supply strategies. Through the synergy of client forecasts and our data-backed expertise, we empower sponsors to make smarter planning decisions—delivering the right supplies to every site, exactly when required.
This approach not only prevents shortages or overstocking but also enhances the overall efficiency of clinical trial execution. With our quality-driven, proactive methodology, Quantime stands as a trusted partner for reliable, efficient drug storage and distribution for clinical trials.
Temperature-Controlled Storage Solutions Across All Ranges
| Category | Temperature Range | Description |
|---|---|---|
Cryogenic | Below -150°C | Ultra-low temperature storage for critical biological samples and materials requiring cryogenic preservation. |
Deep Frozen / Ultra-Low | Below -60°C (e.g., -70°C ± 10°C) | Ultra-low temperature storage for deep-frozen biological materials and sensitive samples. |
Frozen | -25°C to -15°C | Frozen storage for biological materials and temperature-sensitive products. |
Refrigerated (Cold Chain) | +2°C to +8°C | Refrigerated storage for temperature-sensitive pharmaceuticals and biologics. |
Cool Storage | +8°C to +15°C | Cool storage for products requiring moderate temperature control. |
Controlled Room Temperature (CRT) | +15°C to +25°C | Controlled room temperature storage for stable pharmaceutical products. |
Ambient | +15°C to +30°C | Ambient temperature storage for stable products at room conditions. |
Ensuring Excellence in Every Aspect of Storage
At Quantime, our temperature-controlled storage operations are governed by rigorous QA oversight at every step, ensuring strict adherence to established SOPs and unwavering commitment to quality, precision, and regulatory compliance. Every element of our facility is designed to maintain product integrity and ensure seamless clinical supply management.
Process Validation
Our storage processes undergo rigorous validation to ensure they meet GxP & other regulatory and quality standards. Each system is qualified and routinely reviewed to deliver consistent, reliable performance.
Temperature & Humidity Monitoring
We employ advanced, real-time temperature & humidity monitoring systems that continuously track and record environmental conditions, ensuring products always remain within their specified ranges, with an integrated alarm system to detect any deviations.
Daily Records & Emergency Backup
Comprehensive daily documentation and automated backup systems safeguard temperature data and operational continuity. In the event of power or system interruptions, our emergency protocols ensure uninterrupted temperature control and data security.
Segregated Storage Areas
Our facility features clearly defined and segregated storage zones that eliminate the risk of cross-contamination and maintain strict product segregation based on temperature, stability, and study requirements.
These essential aspects form the backbone of Quantime's operational excellence—delivering reliability, compliance, and confidence in every phase of clinical trial drug storage and distribution.
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