June 25, 2024
The line between a safe and effective medication and a dangerous one is often razor-thin. To prevent crossing this line, the United States Pharmacopeia (USP) has established guidelines, such as USP 797 and USP 800. These chapters aim to improve the overall safety and ha...
June 21, 2024
Clean packaging rooms are the last line of defense in keeping products from contamination, at least until they reach consumer hands. These areas are typically less strict than the environments they were manufactured in, but still clean enough that no major issues with g...
Read more about Clean Packaging Rooms: Everything You Need to Know
June 18, 2024
In many industries, controlled environments are important to both improving the safety and quality of products. Both white rooms and cleanrooms are types of controlled environments fit for this purpose; however, each is used under slightly different circumstances. Under...
Read more about White Room vs Cleanroom: What’s the Difference?
June 13, 2024
Did you know that around 8 million healthcare workers are at risk of exposure to hazardous drugs? These risks can include infertility, birth defects, and even certain cancers. As a result, creating a safe environment for personnel is of the utmost importance. And this i...
Read more about What are USP 800 Cleanroom Requirements? Must-Know Facts
June 10, 2024
Have you ever wondered how hospitals prevent infectious diseases from spreading patient to patient, despite being filled with germs? The secret lies in negative pressure rooms, which were used extensively during the COVID-19 pandemic. In hospitals, they help isolate pat...
Read more about What is a Negative Pressure Room? Understanding the Basics
June 6, 2024
Laminar airflow is an important element in many highly-controlled cleanrooms, including operating rooms, semiconductor fabrication plants, biotech labs, and more. But what exactly is it? And how does it contribute to cleanliness in cleanrooms? In the simplest terms poss...
June 3, 2024
Picture a space where the tiniest particle is an adversary. This is not far from the truth, as in many industries, a single particle can cause serious damage to products. To minimize these dangers, many manufacturers use cleanrooms, and these spaces must use cutting-edg...
Read more about Cleanroom Air Flow: Techniques, Pressure Control, and More
May 30, 2024
Good Manufacturing Practice (GMP) cleanrooms are the backbone of quality products in the medical and healthcare industries. GMP standards are usually applied to cleanrooms used in pharmaceuticals, biotechnology, medical device manufacturing, and other related industries...
Read more about What is a GMP Cleanroom? A Comprehensive Overview
May 27, 2024
In some industries, creating high-quality products or research depends in large part on the environment they are conducted in. Organizations may use a variety of controlled environments, such as dry rooms and cleanrooms, to protect these products and processes. In this ...
May 23, 2024
Cleanrooms are necessary in any industry where controlling particles, whether viable or non-viable, is a factor in product safety. Not to mention scientific research, where a clean environment can make the difference between reliable and unreliable results. The needs of...
Read more about What are ISO Cleanroom Standards? Why are They Important?
May 20, 2024
Cleanrooms, and especially ISO 4 cleanrooms, have a lot of complex requirements that can seem difficult at first for a non-technical audience. Fundamentally, though, cleanroom requirements are all about managing airborne particles. The main difference between each ISO c...
Read more about What Are the Requirements for an ISO 4 Cleanroom?
May 16, 2024
In manufacturing, especially in industries that require highly controlled environments, such as pharmaceuticals and food production, following regulations is a necessary step in creating high-quality products. To make sure that products stay safe and consistent, the Foo...
Read more about What is the Difference Between cGMP and GMP?