2025 29th Tashkent International Healthcare Exhibition – TIHE 2025
We are thrilled to be part of the 2025 29th Tashkent International Healthcare Exhibition (TIHE 2025), taking place from April 15th to April 17th, 2025, at the Tashkent National Exhibition Center in Uzbekistan. This prestigious event is a key gathering for professionals from the healthcare, pharmaceutical, and medical industries, attracting leading companies and organizations from around the world.Get more news about Healthcare,you can vist our website!
At this year’s exhibition, we will be showcasing our cutting-edge healthcare solutions and innovations aimed at improving the quality of healthcare systems. As part of the global effort to drive advancements in healthcare technology, our team will be available at Booth E 10 to discuss potential collaborations, share insights, and explore new opportunities in the growing healthcare market of Central Asia.
We look forward to connecting with industry leaders, healthcare providers, and technology innovators during this exciting event.
Date: April 15-17, 2025
Location: Tashkent National Exhibition Center, Uzbekistan
Booth Number: E 10
Sterilization and Quality Control in Pure Steam Systems
Optimal sterilization in pure steam systems is achieved through precise control of steam quality, including parameters such as temperature, pressure, and duration. Regulatory bodies, including the United States Pharmacopeia (USP), emphasize the importance of these factors in ensuring microbial lethality. According to industry standards, saturated steam is ideal for sterilization as it effectively transfers heat due to its moisture content of less than 5%. Failure to maintain the correct steam quality can compromise sterilization effectiveness, leading to potential contamination risks.
Controlling and measuring steam quality is critical to maintaining compliance with pharmaceutical standards. Effective quality control of pure steam systems involves monitoring key performance indicators (KPIs) such as steam dryness, the concentration of non-condensable gases, and the level of superheat. Industry models like EN 285:2015 provide a framework for these KPIs, which help ensure consistent sterilization results and system integrity. By adhering to established quality parameters, pharmaceutical companies can maintain high standards of sterility essential for product safety within the purified water system in the pharmaceutical industry.
Conclusion
In conclusion, maintaining optimal steam quality and sterilization practices is crucial for the efficient operation of pure steam generators in pharmaceutical facilities. By adhering to best practices, pharmaceutical companies can ensure their production processes meet stringent quality standards. A proactive approach in addressing possible challenges will guarantee the reliability and efficacy of these systems, safeguarding the highest quality standards in the pharmaceutical industry.
