Environmental Monitoring for Biomedical Research Labs.
One System. Monitoring, Compliance, Protection.
Built Different. On Purpose.
A failing -80°C freezer doesn’t announce itself. It degrades over weeks — compressor cycles get longer, recovery times slow down. PharmaWatch tracks these patterns and alerts your team to struggling equipment before it fails completely. You replace the freezer on your schedule, not after you’ve lost irreplaceable samples.
Some samples get stored for years. Decades, even. PharmaWatch maintains a continuous, unbroken monitoring record for as long as your samples are stored — with calibration certificates automatically renewed before expiration and every historical reading accessible in 3 clicks.
Data integrity isn’t just a compliance requirement — it’s the foundation of reproducible science. PharmaWatch builds an unbroken, tamper-evident environmental record across every storage unit in your lab, giving you the documentation to stand behind every study and every submission.
GLP Records That Build Themselves.
FDA Good Laboratory Practice (GLP) requires that every nonclinical study be conducted in a well-characterized, controlled environment — and that those environmental conditions be continuously documented. Gaps in your environmental record aren’t just a compliance problem. They’re a scientific integrity problem that can call your entire study into question.
PharmaWatch logs every reading, every alarm, and every corrective action automatically — with timestamps and user IDs. Your environmental documentation builds itself in the background while your team focuses on the research. When an auditor or FDA reviewer asks for your records, your lab manager pulls a complete report in 3 clicks.
Backed by a 100% U.S. based support team trained in regulated healthcare environments — ensuring fast response, expert guidance, and uninterrupted protection.
How PharmaWatch Protects Your Entire Health System.
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