Setra Blog

Setra Systems will be exhibiting at the AHR Expo in Las Vegas from January 31 through February 2. In addition to our extensive HVAC and Critical Environments lines, this year Setra will be unveiling several new and exciting products. Come by and see Setra at booth C5712!

Converting mA to voltage is common in HVAC when working with pressure transducers. Terminology to keep in mind includes:

• 1 mA = 0.001 AMP (short for amperes)
• Amps are referred to as CURRENT
• Resistor values are in OHMS (Ω is the symbol for ohms)
• VOLTAGE is the result of passing amps through a resistor

Cleanrooms are one of the most strictly regulated critical environments that require continuous monitoring. The most common cleanrooms are in compounding pharmacies, medical device manufacturers, and biotechnology facilities, as they need to guarantee the safety of their products for patients. However, a variety of other applications utilize cleanrooms to ensure accuracy, such as clinical research spaces, semiconductor manufacturers, and aerospace manufacturers.

Setra's latest product innovation of wireless transmitters builds on our over fifty years of experience delivering industry leading sensing technology. Our new wireless sensing product line can easily measure and monitor a variety of environmental parameters. Wireless transmitters are used throughout a number of applications, including but not limited to:

The latest version of Setra CEMS, CEMS 5.0, releases on July 20, 2021. Coming with this new version of the software are several new features.

It is commonly assumed that organizations need to choose between NIST and ISO. Neither is better than the other and can both be used simultaneously.

Maintaining and monitoring room pressurization in hospitals is essential for meeting regulatory standards and ensuring the safety of a space. Incorrect room pressurization jeopardizes the health of both patients and staff.

Air scrubber and negative air machine are two terms commonly used interchangeably. However, there is a difference between the two, as they are designed for different applications.

Cleanrooms for medical device and pharmaceutical manufacturing are highly regulated spaces and there are numerous standards that need to be considered. When it comes to how data is handled in regulated cleanroom environments, the United States FDA issued 21 CFR Part 11 guidance that should be followed closely.

Throughout the COVID-19 pandemic, there has been an emergence of new technologies advertised for helping remove the pathogen from the air. However, these methods have major flaws that present significant implementation challenges or make them ineffective at preventing the spread of COVID-19.