TempTrail™ Display (Single/Multi-use Temperature Datalogger with Display)
- -30°C to +70°C for IMP storage & transit
- Tamper-evident PDF records per site
- FDA 21 CFR Part 11 & DO-160G certified
FDA 21 CFR Part 11
DO-160G Certified
CE & RoHS Compliant
Clinical Trial Temperature Data Loggers by Realog View are FDA 21 CFR Part 11 compliant devices designed for precise, traceable temperature monitoring across pharmaceutical cold chains, vaccine transport, cryogenic storage, and laboratory environments. With automatic PDF/CSV reporting, no external software required, and IP67/IP68-rated housings, these loggers ensure data integrity across every stage of clinical operations.
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Yes. All Realog View TempTrail data loggers are FDA 21 CFR Part 11 compliant, ensuring secure, tamper-proof electronic records with full audit traceability. This makes them suitable for regulated clinical trial environments where data integrity and validated processes are mandatory requirements.
Talk to our experts for custom solutions and tailored guidance.
Ensures FDA-compliant, traceable temperature records for drug storage, biologics, and clinical trial shipments.
Monitors temperature integrity of vaccines and biologics across cold chain shipments and distribution.
Tracks ultra-low temperatures down to -85°C for cryogenic freezers, dry ice shipments, and biorepositories.
Provides reliable environmental temperature monitoring for laboratory equipment, reagents, and critical medical supplies.
Protect vaccines, biologics, blood products, and clinical trial samples with audit-ready temperature records across labs and hospitals.
Validate curing, sterilization, reflow, and coating processes across medical device, electronics, semiconductor, aerospace, chemical, and automotive production.
Hold precise fermentation, mashing, barrel-ageing, and cellar temperatures to protect batch consistency and flavour profile.
Track temperature and humidity across greenhouses, grain stores, and post-harvest handling to maximise yield and reduce spoilage.
Maintain stable conditions for artworks, archives, and artefacts in museums, galleries, and hotel storage and display spaces.
Continuous oversight of cold storage, commercial warehouses, and data centre and IT infrastructure to prevent downtime and stock loss.
Talk to our experts for custom solutions and tailored guidance.
Every data logger generates tamper-proof, traceable PDF and CSV records meeting FDA 21 CFR Part 11 requirements for clinical and pharmaceutical audits.
Automatic report generation via USB with no external software needed, reducing IT burden and accelerating compliance documentation across clinical sites.
A comprehensive product range spanning ultra-low cryogenic to high-temperature autoclave monitoring, covering every clinical trial storage and transport scenario.
Submit your requirements and our team will respond with product recommendations, compliance details, and pricing within one business day.
You can also send us a quick email at contactus@realogview.com.
You can also send us a quick email at contactus@realogview.com.