Laboratory Equipments

Stability Test Chambers are especially designed to conduct stability and shelf life studies on drug and drugs substances. In addition to this, Stability Test Chambers are extensively used for seeds testing, biological studies, testing on electronic & mechanical components, Cement plants, packing industries etc. Chambers conform to International Standards such as ICH, WHO Guideline, and USFDA requirements.

Special Features :

• Precise control of temperature and humidity by using CE approved micro controller based
• PID controller (Imported, Auto tuning type.).
• Direct digital read-out of % RH with a electronic capacitance type sensor. No wick, cup and water (Optional).
• Refrigeration system with CFC free compressor and R-134a ECO- friendly refrigeration system with time delay.
• PC interface with Windows based communication software. (Optional)
• Micro controller based programmable timer for chamber illumination. (Optional).
• Foamed - in - place PUF insulation ensures temperature stability and reduced energyconsumption.
• Audiovisual alarm if the temperature deviates from the pre set temperature (Optional).

Cabinet Construction and Refrigeration System :
The cabinet of Chambers are insulated with high density CFC free Poly Urethane Foam. Interior of chambers is mirror finish stainless Steel (304 SS, 0.8 mm thick). The exterior is white powder coated (1.0 mm thick) mild steel and the door has magnetic gasket with a keyed door lock. Stainless steel trays are provided for storage inside. The cooling is effected by hermitically sealed compressor of high quality. GMP models are in total stainless steel (Inside S. S 316 with mirror finished and outside. S 304 dull finish.) is also manufactured by Skylab.

Optional Accessories:
Stand by Refrigeration system Ready to use stand by refrigeration system in case of regular system fails. This includes Compressor, Evaporator, condensers and other accessories.

Safety controller :
Dedicated safety controller with separate sensor to switch off the power supply in case of overshoot and undershoot of temperature giving audio visual alarm.

Data scanner :
Data Scanner 4 point temperature and 4 point humidity or 8 point temperature 8 point humidity complete with Sensors and printer interface and data storage facility.

Printer Interface :
Facility to store, print records on printer with set values, process values, date and time with variable print time interval. Data storage facility to print the data online and offline, suitable for 80 col. Dot matrix printer. Printer interface for LUX & UV meter atomatic shut off after specified exposure level

Software :
CFR 21 Part 11 compliance web based communication software for data management. Complete with RS 485 multi dropping to monitor multiple chambers to one software

PC Interface and data management :
PC Interface with communication allows remote monitoring and data logging to control the chamber. Web based software having reports in tabular as well as graphical form.

Temperature & Humidity Sensor :
Electronic capacitance type Temperature & Humidity Sensors, which will avoid wick, cup and water

PLC system :
For auto changeover of standby systems and other event managements with 3.7" LCD display with touch screen security lock for prevention of unauthorized tampering.

US FDA 21 CFR Part 11 Features :

• Set and view control parameters
• Complying US FDA 21 CFR Part 11
• Access Control and different access levels
• Multi user with individual user name and password
• Database protection, backup and restore facility
• Online and offline trends
• Chamber wise report / trend generation, printing facility reports can be export to other formats (PDF, Excel)
• Analysis of stored data
• Alarm acknowledgment with user comments
• Auto logout and account lockout facility
• Access control with unique username and password
• Reconfirmation of username and password for change of critical parameters alphanumeric password
• Password aging complying US FDA 21 CFR Part 11 Date and Time stamp audit trails user equipments
• Alarms SMS audit trails seaparate alarm and log data recording SOP for installation backup, restore, software operation.

Documentation :
For GMP complaint models offers IQ, OQ, PQ and DQ validation with documentation, reports, calibration and test certificates

Calibration :
The equipment is calibrated with the help of master calibrator, which is certified for its accuracy by Electronics Regional Testing Laboratory (ERTL West) Government of INDIA recognized testing laboratory with traceable reference to National Physical Laboratories (NPL)