characteristic:

-Can achieve a temperature of -10~100 degrees Celsius and a humidity of 10% RH~95% RH

-5-level automatic defrosting function, stable and stable temperature and humidity, meets GMP and FDA requirements for frost free operation (above 20 degrees)

-Log recording, audit tracking function

-Total control function for illuminance and ultraviolet light intensity (based on pharmacopoeia 1.2 million LUX strong light and near ultraviolet light 200W.hr/m2 total control)

-Equipped with electronic signature function that meets FDA requirements, ensuring more objective test data

-Real time data recording and export function (USB encrypted export or upper computer serial port export)

-Fault monitoring, alarm, recording, and export functions (USB export)

-Level 4 password function: login password, operator password, administrator password, advanced administrator password

-Three power failure mode selection functions: power failure recovery, stop or restart

-Historical data and historical curve query and download function

-Maximum support for expanding 16GTF memory card, capable of storing data for at least 10 years;

-Environmental temperature detection function

-PDF data export function (exported through upper computer software)

-The computer monitoring software has monitoring and synchronization control functions, which can support simultaneous control of 20 devices (PTH-LQC series does not have this function)

-GPRS SMS alarm function

-Water level monitoring and automatic water replenishment function

-Can provide communication protocols and connect to the comprehensive equipment management platform of pharmaceutical companies

Lighting system:

Meet the requirements of ICH (Q1A and Q1B) guidelines and comply with the guidelines for drug stability testing in the National Pharmacopoeia.

Visible light (VS) D65 light source, 4500 ± 500lux, 320-400nm wavelength near ultraviolet light (UV); Adjustable light intensity, light and ultraviolet radiation tests can be completed simultaneously.

Visible/ultraviolet light detection sensor:

computer monitoring software

Optional computer monitoring software, compatible with the data interface of the comprehensive equipment management platform of pharmaceutical companies, capable of providing data access for review requirements, audit tracking, and electronic signatures

Temperature and humidity range:

Complies with the pharmacopoeia guidelines for drug stability testing at 40 ° C/75% RH or 30 ° C/60% RH for 180 days

25 degrees/60% RH or 30 degrees/60% RH 365 days

Easy to operate and use: