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Automated Monitoring Built for Regulated Enviroments

Temperature, humidity, CO2, LN2 Levels and more.

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Automated Calibration — swap the probe in 60 seconds, no service visit, no monitoring gap
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Installs in under 20 minutes — plug it in and it's running, no IT team needed
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Always Audit Ready every reading logged automatically, full compliance reports in 3 clicks
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Monitoring Critical Enviroments All Over the World
Our features

Built for Critical Environments. Trusted for Compliance.

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Every Parameter. Not Just Temperature.
We monitor what your environments actually require — temperature, humidity, CO₂, differential pressure, Liquid Nitrogen (LN₂) depth, open door detection, and flood and wetness protection. All of it. One system.
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Know the Moment Something Changes
Every 5 minutes, data from every sensor hits our globally redundant cloud. Temperature spike, humidity drift, Liquid Nitrogen (LN₂) level drop, power loss — you know about it in minutes. Not hours.
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Alerts That Always Find a Human
Three-tier Smart Alert escalation via call, text, or email. First person doesn’t respond? The next one gets it automatically. Nobody misses an alarm because they stepped away.
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Thresholds That Fit Your Environment
A blood bank refrigerator isn’t a cryogenic tank. Set precise alert parameters per zone, per product type, per department — so every alarm earns the attention it gets.
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See Failures Coming
Predictive analytics flag equipment that’s starting to struggle weeks before it fails. You fix it on your schedule — not when the freezer dies at 2am.
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One Dashboard. Every Location.
Single facility or 50-site enterprise — every sensor, every alert, every reading in one dashboard. 3 clicks to any data point, from any internet-connected device.
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View Compliance Documentation
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Talk with a monitoring expert
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Why real-time monitoring matters

Single Excursion Can Change Everything.

A single undetected excursion can compromise years of research, destroy irreplaceable biological material, or trigger an FDA investigation that shuts down your operation. These aren’t hypotheticals. They happen — mostly to facilities that were monitoring manually, or on WiFi that went down at the wrong moment.

PharmaWatch was built so that never happens to you. Whether it’s a hospital pharmacy, a blood bank, acryogenic storage facility, or a vaccine clinic — every environment is watchedcontinuously, every reading is logged automatically, and every excursion triggersan alert that finds a human before the product is lost.

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$35B+ in temperature-sensitive products lost annually due to cold chain failures (WHO)
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26% of vaccines arrive damaged due to temperature excursions
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100% of FDA inspections review temperature monitoring records
Environments we monitor

Whatever You're Storing, We Monitor it.

01.
Refrigerators & Freezers
Protect vaccines, biologics, blood products, and pharmaceuticals in standard refrigerators and freezers. Continuous monitoring with tamper-proof records and Smart Alerts that fire before a product is at risk.
02.
Ultra-Low Temperature (ULT) Freezers
Monitoring at -80°C and below for irreplaceable samples, cell therapies, and long-term biospecimen storage. Predictive analytics flag equipment degradation before a catastrophic failure occurs.
03.
Liquid Nitrogen Tanks
Real-time Liquid Nitrogen depth and level monitoring. Vacuum loss detected in approximately 25 minutes. Alerts fire before levels approach critical — not after specimens are already compromised.
04.
Incubators & CO₂ Incubators
Simultaneous monitoring of temperature, CO₂, and humidity. Everything cell cultures, embryos, and biological samples depend on — tracked continuously and logged automatically.
05.
Cryogenic Storage
Continuous monitoring from -196°C to -80°C. Every reading logged automatically with timestamps and user IDs for FDA HCT/Ps, Current Good Tissue Practice (CGTP), and CAP compliance.
06.
Cold Rooms & Walk-In Units
Multiple sensors per space eliminate monitoring blind spots. Zone-by-zone visibility with tamper-evident data accessible from any internet-connected device at any time.
08.
Vaccine Storage Units
Refrigerated (2°C–8°C) and frozen (-50°C to -15°C) vaccine storage with automated temperature logs that satisfy CDC Vaccines for Children (VFC) and state immunization program requirements.
09.
Warehouses
Ambient temperature and humidity monitoring across large-scale pharmaceutical storage and distribution environments. Enterprise-wide visibility from a single dashboard.

Compliance Standard We Support:

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FDA GxP, cGMP, and Good Laboratory Practice (GLP)
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FDA 21 CFR Part 11 — Electronic Records and Signatures
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FDA Human Cells, Tissues, and Cellular Products (HCT/Ps)
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FDA Current Good Tissue Practice (CGTP)
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AABB (American Association of Blood Banks)
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CAP (College of American Pathologists)
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Joint Commission (JCAHO)
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CLIA (Clinical Laboratory Improvement Amendments)
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USP 797/800 — Pharmaceutical Compounding
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CDC Vaccines for Children (VFC) Program
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State Board of Pharmacy
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NIST-Traceable Calibration / ISO 17025
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IQ/OQ/PQ Validation — Included in Every Deployment
Compliance on autopilot

Automated. The Way Compliance Should Be.

PharmaWatch sensors connect to our secure cloud over dedicated cellular networks — not your hospital’s WiFi. No IT involvement. No firewall changes. No new attack surface on your network. Data transmits encrypted every 5 minutes, building a continuous, tamper-evident record that holds up under the toughest regulatory scrutiny.

The platform is built oninfrastructure designed to support FDA 21 CFR Part 11 requirements — withredundant data storage, role-based access controls, and an audit trail thatlogs every user action, every alarm acknowledgment, and every system change. Fromthe sensor to the inspector’s report, every data point is secured, timestamped,and traceable.

Grow with ease

More Locations. Same Confidence.

One facility becomes ten. One blood bank becomes a regional network. PharmaWatch scales without adding IT burden, implementation timelines, or compliance risk. New sensors deploy in under 20 minutes. Your dashboard just gets bigger.

Every new deployment comes with a comprehensive Validation Report reviewed by PharmaWatch’s own experts. Your compliance posture keeps pace with your growth — automatically.

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Backed by a 100% U.S. based support team trained in regulated healthcare environments — ensuring fast response, expert guidance, and uninterrupted protection.

Our team is here for you.
24/7 • 365
Happy Customers
98% NPS Score
Frequently ask a questions

Find the answers here

What types of equipment does PharmaWatch monitor?
PharmaWatch monitors any temperature-sensitive storage unit, ULT freezers, standard refrigerators, incubators, cold rooms, cryogenic tanks, and ambient storage areas. If it stores something regulated, we monitor it.
How quickly will I be alerted to a temperature excursion?
In under 60 seconds. PharmaWatch uses multi-tier alarm escalation, call, text, and email, to ensure the right person is notified immediately, no matter the time of day.
Is PharmaWatch compliant with FDA 21 CFR Part 11?
Yes. PharmaWatch is built for FDA 21 CFR Part 11 compliance out of the box, with tamper-evident logs, user attribution, timestamped records, and audit-ready report generation.
Do I need an IT team to install PharmaWatch?
No. Sensors arrive pre-configured and connect via cellular, not your WiFi network. Most facilities complete installation without any IT involvement in a single day.
What happens if my internet goes down?
PharmaWatch operates over cellular, not your internet connection. Sensors store data locally and sync automatically. You never lose data, and your team is alerted before you even notice an issue.
What happens if my internet goes down?
PharmaWatch operates over cellular, not your internet connection. Sensors store data locally and sync automatically. You never lose data, and your team is alerted before you even notice an issue.
Can PharmaWatch scale across multiple locations?
Absolutely. Whether you're monitoring 3 sensors in a single clinic or 300 units across a health system, PharmaWatch scales with you, all managed from one centralized dashboard.
Is IQ/OQ/PQ validation documentation included?
Yes. Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) documentation is included in every PharmaWatch deployment at no additional cost — not sold as a separate professional services engagement. Documentation is prepared and delivered during onboarding so your validation package is ready before your system goes live.

Protect What You Can’t Afford to Lose.

Our team will walk you through a live demo tailored to your facility — your equipment, your compliance requirements, your timeline. No generic slide deck.

90 Day Satisfaction Guarantee
No Upfront Costs
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