Report and analyze real-time environmental data from your critical assets. Automated compliance reports, instant alerts, and cloud dashboards — 24/7 visibility for pharmaceutical, biotech, and clinical labs.
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ARTEMIS remote monitoring is the continuous, automated surveillance of environmental conditions in laboratories, cold storage, and GxP facilities. Networked wireless and wired sensors sample temperature, relative humidity, differential pressure, and CO2 at fixed intervals around the clock, log every reading to a secure cloud platform, and raise immediate SMS and email alarms the moment a value drifts outside its configured limits. Continuous monitoring is distinct from calibration — the periodic NIST-traceable verification of a sensor’s accuracy — and from a temperature-mapping study, which characterizes spatial distribution at a single point in time. Monitoring protects stored product between those events by giving you a live, uninterrupted, audit-trailed record of the conditions your samples actually experienced.
ARTEMIS monitors the full range of critical environmental parameters. Temperature is tracked across ultra-low (−80 °C) and −20 °C freezers, refrigerators, cryogenic liquid-nitrogen (LN2) storage, incubators, ovens, stability chambers, and ambient rooms using wired thermistor, RTD, and thermocouple probes as well as self-contained wireless sensors. Relative humidity is monitored in cleanrooms, stability chambers, and controlled storage; differential pressure is monitored across cleanroom, isolator, and containment suites in pascals (Pa) or inches of water column; and CO2 is monitored in cell-culture incubators. ARTEMIS also captures door and contact-closure events and accepts generic analog (4–20 mA, 0–10 V) and digital sensor inputs, so a single platform covers virtually any measurable condition in your facility.
Each ARTEMIS sensor samples its parameter at a configurable interval — typically every 1 to 15 minutes — and transmits the reading wirelessly to a gateway or over the wired network to the secure cloud, where it is stored with a timezone-aware timestamp. Every monitored point carries configurable high and low limits plus a delay filter that suppresses nuisance alarms from brief, expected excursions such as a door opening or a defrost cycle. When a reading breaches its limit for the configured duration, ARTEMIS raises an alarm by SMS, email, and voice call, and escalates to additional on-call contacts if the alarm is not acknowledged. Local data buffering and battery-backed sensors keep the record intact through network and power interruptions, so no readings are lost during an outage.
Yes. Calibration and monitoring are distinct activities, and ARTEMIS covers both. Every temperature, humidity, differential-pressure, and CO2 sensor is calibrated in Femto Scientific’s ISO/IEC 17025 accredited laboratory against NIST-traceable reference standards and is documented on a certificate reporting as-found and as-left data with expanded measurement uncertainty (k=2, 95%). Because a monitoring sensor drifts with age and use, it is recalibrated on a periodic interval — typically every 12 months — to prove its readings remain accurate, then returned to continuous service. Femto manages the recalibration schedule for your fleet and performs it onsite or by calibrated hot-swap sensor, so your facility keeps an unbroken monitoring record with no coverage gap during the calibration event.
Yes. The ARTEMIS cloud platform is designed to support FDA 21 CFR Part 11 electronic records and electronic signatures. Access is controlled by unique, role-based user accounts; a secure, time-stamped audit trail records every reading, configuration change, alarm, and user action; and alarm acknowledgements and annotations are captured as attributable electronic signatures. Stored records are tamper-evident and retained for the required period — they cannot be silently altered or deleted. Scheduled reports are formatted for GxP and cGMP, WHO Good Distribution Practice, CAP, CLIA, and CDC Vaccines for Children documentation. ARTEMIS supplies the compliant system and the IQ/OQ/PQ qualification records; your organization defines the SOPs and signature meanings that complete a Part 11 program.