Temperature monitoring for the pharmaceutical industry

Temperature monitoring for the pharmaceutical industry
Medicines, vaccines, samples, and raw materials must be stored between +2 °C and +8 °C (or according to their specifications) during both storage and transport.

JRI designs IoT solutions for temperature/humidity monitoring: wireless sensors, data loggers, real-time alerts, and secure cloud platforms. The systems comply with ISO 17025, ISO 15189, and Good Manufacturing and Distribution Practices (GxP).

Your Specific Needs

Simplicity

Intuitive interface for real-time monitoring and quick adoption by your teams. Dashboards in MySirius designed for Quality/Production teams: real-time views,…

Security

Protect the integrity of your critical data with enhanced JRI security, adapted to pharmaceutical requirements.
Our compliant archiving systems make…

Compliance

Validated systems GMP/GDP, ISO 17025 and ISO 15189; IQ/OQ/PQ files provided by JRI teams. Configurable alarms (+2 °C/+8 °C, –20…

Reliability

Eliminate any risk of data loss with JRI pharmaceutical-grade reliability.
Our high-precision sensors and redundant architecture operate continuously, even in…

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Modules and Applications

Module Cleanroom

The Cleanroom Module is a customised solution designed for real-time monitoring of cleanroom environments. It adapts to your critical installations.

Plans Module

The Plans Module facilitates pharmaceutical equipment management. Visualize your storage areas and cold rooms in real time for centralized monitoring and simplified compliance audits.

Maintenance Module

The Maintenance Module optimizes pharmaceutical equipment reliability. Schedule interventions, track history, and ensure metrological traceability compliant with GMP.

Calibration Module

With the Calibration Module, ensure the accuracy of temperature and humidity probes. Manage certificates, comply with ISO 17025 requirements, and simplify quality controls.

Mapping Module

The Mapping Module ensures the safety of drugs and vaccines. Perform temperature and humidity mapping to demonstrate regulatory compliance and validate your storage units.

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Our Services for the Pharmaceutical Industry

Technical Support and Maintenance

Fast assistance online or on-site to resolve issues and minimize downtime.

Installation and Commissioning

Equipment installation with user training and knowledge transfer to achieve autonomy.

On-site
Metrology services

Professional metrology delivered directly to your premises with laboratory-grade precision.

Laboratory Sensor Calibration

Metrological services to ensure compliance and accuracy of your measuring instruments.

Our Customer Testimonials

Benoit Lancelin
Pharmacist Biologist

How Biosite revolutionised its cold chain monitoring with JRI MySirius Mobility

Transporting biological samples is a race against time, where every degree counts. For Biosite, a medical analysis laboratory located in the heart of Maine-et-Loire, this reality had become a constant challenge. Discover how adopting JRI’s MySirius Mobility solution transformed their operations, simplifying temperature management and strengthening traceability.

DYNALAB chooses the JRI-MySirius solution

Read the case study
Sofien Dessolin
President Cell&Co

Preservation of biological samples: Cell&Co masters the cold chain with JRI-MySirius

Centralize and preserve collections of temperature-sensitive products Specializing in the management of GMP (Good Manufacturing Practice) products, as well as those of biological and chemical origin, Cell&Co meets the needs of its industrial clients and life sciences laboratories by leveraging the JRI-MySirius solution to secure storage conditions and ensure the traceability of temperature data.

A question ?

What regulatory requirements does MySirius cover?

The Advanced level is compliant with 21 CFR Part 11: tamper-proof audit trail, electronic signatures, and GxP access profiles. Data is archived for 10 years to meet GMP and FDA inspections.

How do you manage IQ/QO validation?

JRI provides audit-ready IQ/OQ protocols; a metrologist accompanies the functional tests of enclosures (cold roomstabilothèque). Signed reports are stored in MySirius for each equipment.

 

Does JRI offer qualification and validation services for pharmaceutical equipment?

Yes, JRI offers comprehensive support for pharmaceutical equipment qualification:

Qualification services:

  • Qualification of freezers and storage enclosures in accordance with Good Distribution Practices
  • Thermal characterization of enclosures from -196°C to +200°C via its COFRAC laboratory
  • Validation of performance and stability of refrigeration equipment

Specialized expertise:

  • Collaboration with CIET Pharma, specialized in pharmaceutical and cosmetic equipment control
  • Reports compliant with health authority requirements
  • Dedicated technical support for the pharmaceutical industry

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