Ziebaq is one of the best companies in Saudi Arabia for validation services. Our reputed organization provides services throughout and internationally. Ziebaq has used the thermocouples and the thermistors for many years. A lot of rules and regulations govern the pharmaceutical business. These rules are based on study, evidence, keeping records, and validation. With our knowledge and experience, we can give you a clear validation package that follows the rules and is honest. A process called "thermal validation" ensures that storage facilities and equipment will work as expected and maintain the temperatures they are made for. Contact us for the best thermal validation services.
With Ziebaq, you can get custom options for thermal validation studies that focus on cleaning and disinfection processes. Our thermal validation services ensure that autoclaves and other equipment work correctly and are in line with rules and laws worldwide. What we offer:
Cold rooms, freezers, refrigerators, and cryogenic tanks can all use Ziebaq to help with their temperature validation. We look at temperature maps and, if needed, relative humidity maps of your systems and places to ensure they meet your acceptance standards. We look at how the temperatures are spread out in your systems to find the most typical or worst-case spots for tracking. This ensures that time- and temperature-sensitive pharmaceutical goods are stored in the best way possible. We can also test the system for robustness against possible problems by leaving the door open and turning off the power.
Control over autoclaves and other cleaning methods is essential, but the quality of your steam is also very important. Testing for EN 285 gives useful information, and the High Council of Public Health suggests doing it every year to check the steam quality. Problems like too many gases that don't condense, poor heat transfer, and too hot steam can all make cleaning less effective. Ensuring that your cleaning methods meet the highest standards helps avoid issues like low steam penetration power, ineffective or incomplete sterilization, and wet loads.
Flexible endoscopes offer many technical options, which makes cleaning and sanitizing them more difficult. The best method is mechanical, requiring a carefully managed process. Hospitals must show that all equipment used in the sterilization or disinfection processes works properly to meet the standards for JCI or NIAZ approval. The endoscopy department's devices, which need a clean scope, must also be confirmed. Endoscopes are cleaned and disinfected thoroughly during validation, and the right way to dry and store them is also confirmed. Due to their fundamentally different use and construction, endoscopes require a customized validation tool to ascertain their effectiveness.
Thermal validation tests prove that environments or goods sensitive to temperature are being watched and recorded properly.
In thermal validation, goods are heated to high temperatures to sterilize or do other processes.
A few important factors, such as accurate temperature and humidity readings and accurate cycles within set limits, are usually checked during temperature-controlled chamber validation.
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