Description

Temperature Verification Software Power 3000

 

calibration

● Multi-point calibration, single-point or multi-point calibration can be achieved

● Various wired calibration modes, including manual or manual + automatic mixed calibration

● In the fully automatic calibration mode, it can automatically communicate with the probe or dry well to automatically complete the calibration

● Support multi-stage compensation and calibration of wireless recorders

● With post-verification function

verify

 

● Supports three types of verification: temperature, humidity, and pressure. The verification channel can be expanded infinitely

● Support wired, wireless, and hybrid (wired + wireless) authentication methods

● Support multiple verification start and stop methods

● Can run verification on multiple devices in real time, with no limit on the number of verifications

● Wired verification can observe verification data in real time: trend chart, kill rate calculation, temperature statistics calculation, etc.

● During wireless verification, you can close the software after running it in the background

Report

 

● Both calibration and verification can generate original unchangeable calibration data and verification data

● Calibration data can be split into multiple reports as needed

● Verification data can be divided into multiple cycles and multiple stages

● Report content can be flexibly filtered to display important information

● Different parameters can be set to calculate F0 value, FH value, A0 value, etc.

● Calculate cold spots, hot spots, uniformity, fluctuation, etc.

● The verification report calculation content is comprehensive and rich, meeting different calculation needs

● Calibration or verification data can be backed up and restored separately

● Can output files in different formats such as PDF, CSV, Excel, etc.

● Detailed report filtering capabilities

Compliance and Security

 

● Comply with FDA 21CFR Part 11 requirements for electronic records, audit trails and electronic signatures

● Comply with EU EN554:1994 on the validation and routine control requirements of moist heat sterilization of medical devices

● Level 3 user management authority

● Audit trail, detailed log tracking records can be used to check every step of the user’s actions

● Detailed log filtering function, convenient for viewing operation records

● Safely back up data offsite