Pharma cold chain monitoring
Scan QR data loggers into cloud reports for medicines, vaccines, samples, and clinical trial materials.
- GDP compliant shipment evidence
- 21 CFR Part 11 compliant cloud records
- Audit trails, certificates, alerts, and release-ready reports
- Data securely uploaded online. No apps needed
Compliance proof that travels with every shipment
QR scans, cloud reports, audit trails, certificates, and validation materials stay connected from dispatch to QA review.
GDP compliant distribution evidence
Reports, scan history, and deviation context for release and partner review.
21 CFR Part 11 electronic records
Audit trails, permissions, secure access, and controlled documentation.
Validation and calibration documents
Validation materials and logger certificates stay connected to the record.
GMP Annex 11 and access control
User access, edit history, secure controls, and exportable reports.
Industry solution
Pharmaceutical temperature monitoring built around quality risk.
Logmore connects the full monitoring loop: QR data loggers collect trusted condition data, Logmore Cloud turns it into reports and dashboards, and the API brings the evidence into enterprise workflows.
For pharma & life sciences, condition monitoring has to bridge the physical shipment and the quality record. Logmore brings pharma cold chain temperature monitoring, scan-first data capture, secure cloud review, and integration-ready evidence into one repeatable workflow for regulated supply chains.
Domestic distribution
Reusable monitoring for domestic pharma lanes
Use QR data loggers again and again on recurring domestic routes for a low cost per mission. The loggers are temperature agnostic, so the same recorded data can even produce multiple product-specific reports when different products travel in one shipment.
International distribution
Single-use or multi-use options for global pharma shipments
Choose single-use loggers when returns are impractical or multi-use loggers when the route supports recovery. Both options fit international pharma and clinical trial shipments where evidence, reports, and deviation review need to reach Logmore Cloud.
Common use cases
- Secure and always available online access to reports
- Easily share and export reports when needed
- Vaccine, biologics, samples, and clinical trial material shipments
Monitoring needs
- Temperature-agnostic logger use across cold chain, CRT, dry ice, and deep-cold lanes
- Multiple reports from the same temperature data when different products share one shipment
- Temperature excursions, time outside limits, and release-ready deviation context
- Audit trails, calibration certificates, validation documentation, and electronic records
Why Logmore
- Reusable loggers for low cost per mission on recurring lanes
- Temperature-agnostic data for cold chain, CRT, dry ice, and deep-cold shipments
- Multiple product-specific reports from the same shipment data
- Single-use and multi-use options for domestic, international, and clinical trial shipments
Product stack
The new standard for pharma shipment monitoring.
Logmore replaces traditional USB data loggers with a more secure, easy-to-use, and scalable cloud-based workflow: scan the QR logger, upload evidence online, review reports in Logmore Cloud, and automate the flow through integrations when your operation grows.
QR data loggers
No USB readers or installed apps
Replace manual USB retrieval with QR data loggers that upload shipment evidence securely online through a phone scan.
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Logmore Cloud
Cloud reports instead of local files
Logmore Cloud keeps reports, alerts, audit trails, calibration certificates, and dashboards available for every team that needs the shipment record.
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Logmore API
Scale beyond manual handling
Connect mission setup, measurements, alerts, comments, and exports to quality systems, control towers, WMS, or TMS workflows.
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Logmore fit
From shipment condition data to decisions, evidence, and action.
The solution combines sensor-equipped QR data loggers, secure Logmore Cloud reports, calibration documentation, alerts, dashboards, and API automation.
QR data loggers for regulated lanes
Logmore data loggers collect temperature and other condition history without requiring scanners, gateways, or new apps in the field. One logger can support multiple shipment profiles and easy upload of data ensures you'll get visibility instantly upon shipment arrival.
QR data loggers for regulated lanes
Logmore data loggers collect temperature and other condition history without requiring scanners, gateways, or new apps in the field. One logger can support multiple shipment profiles and easy upload of data ensures you'll get visibility instantly upon shipment arrival.
- Temperature-agnostic logger use across cold chain, CRT, dry ice, and deep-cold lanes
- GDP compliant shipment evidence
- Secure and always available online access to reports
Cloud reports for quality review
Logmore Cloud turns logger data into readable shipment reports, dashboards, deviation views, audit trails, and documentation records so QA teams can assess whether a delivery stayed inside the required conditions.
Cloud reports for quality review
Logmore Cloud turns logger data into readable shipment reports, dashboards, deviation views, audit trails, and documentation records so QA teams can assess whether a delivery stayed inside the required conditions.
- Multiple reports from the same temperature data when different products share one shipment
- 21 CFR Part 11 compliant cloud records
- Easily share and export reports when needed
API automation for regulated operations
The Logmore Cloud API can start and end Missions, pull collected data into third party systems and reduce manual warehouse steps when regulated logistics workflows need repeatability at scale.
API automation for regulated operations
The Logmore Cloud API can start and end Missions, pull collected data into third party systems and reduce manual warehouse steps when regulated logistics workflows need repeatability at scale.
- Temperature excursions, time outside limits, and release-ready deviation context
- Audit trails, certificates, alerts, and release-ready reports
- Vaccine, biologics, samples, and clinical trial material shipments
Operational workflow
A practical monitoring journey from setup to quality review.
Logmore can support lightweight scan-based flows as well as more automated enterprise processes where Missions are created, ended, and exported through API connections.
Configure the shipment profile
Set the Mission template, logger type, temperature range, alert rules, and documentation requirements before dispatch.
Monitor the journey
The QR logger records condition history in transit. Scans upload data to Logmore Cloud, where deviations, bottlenecks, and trends become visible.
Review and document
Quality teams review graphs, audit trails, calibration certificates, and exportable reports, then use the evidence for release, investigation, or partner communication.
FAQ
Pharma & Life Sciences monitoring questions
Short answers for search visitors comparing temperature monitoring, humidity and shock monitoring, compliance documentation, and business-driven quality control.
Is Logmore suitable for GDP/GMP environments?
Yes. Logmore is built for regulated temperature monitoring workflows with shipment reports, calibration certificates, audit trails, controlled documentation, and secure cloud records that support GDP and GMP expectations.
Does it support 21 CFR Part 11 / Annex 11 needs?
Yes. Logmore Cloud supports workflows aligned with 21 CFR Part 11 and GMP Annex 11 needs, including electronic records, audit trails, permission management, encrypted connections, edit logs, and controlled access to shipment evidence.
Can it be validated for regulated workflows?
Yes. Logmore can support customer validation work with validation materials, calibration documentation, and consistent workflow evidence. The final validation belongs to the customer's regulated process, user requirements, and quality system.
How do audit trails and permissions work?
Logmore Cloud keeps audit-ready records with edit history and controlled access. Permissions help define who can view, manage, share, or review shipment reports, so quality, logistics, partner, and customer access can be handled without opening the full workspace to everyone.
Can it be used for product release?
Yes, Logmore reports can support product release review by showing temperature history, excursions, scan events, calibration certificates, and deviation context. The actual release decision remains with the customer's qualified quality process.
Do you support self-hosted or cloud deployment?
Logmore is delivered as a secure cloud platform with EU cloud data residency. If a regulated workflow requires a specific deployment, data residency, or integration model, the Logmore team can review those requirements during solution design.
Build the right monitoring workflow for Pharma & Life Sciences.
Talk with Logmore about the logger model, thresholds, reports, validation package, and integration pattern that fits your shipments.