A Quick Guide to Training to Ensure Cleanroom Best Practices
Drug development involves a huge investment. According to Wikipedia, a new study published in 2020 estimates that the average cost of drug development is around $ 1.3 billion that includes the cost of drug discovery, clinical trials, approvals and finally...
A Quick Guide to know your Cleanroom Panel – Insulation
A few months back (before the lockdown), a visit to the client drew my attention about how little was he aware of Modular Panels, even though he had signed a project on Cleanroom. Today's blog post is inspired by that...
A Quick Guide to know your Cleanroom Outer Panel
Modular panels are a very crucial part of the cleanroom environment as they create a physical barrier between the controlled cleanroom area and contaminated area majorly, as well as between two different class of cleanroom areas. Modular panels offer factory...
How can Mobile BioContainment Laboratory (Fab- MO DOTS) help you overcome low...
Globally, countries have been unable to pull the leash to contain the spread of Coronavirus that is galloping at a breakneck speed. Most countries across the world have seen a surge in the number of COVID-19 positive cases. A few...
What are the Best Behaviour Rules that Pros follow in a Cleanroom?
Cleanrooms are highly specialised infrastructure conventionally used for manufacturing in Pharmaceutical, Biotech, Healthcare, Semiconductors, Nanotechnology and other industries to control the airborne particles that can be hazardous to the end product and the operator working in the environment. Cleanrooms demand...
Our tips on selecting the right containment system for pharma
Prevention of cross-contamination with highly potent active pharmaceutical ingredients (HPAPI) is a crucial part of a safe manufacturing process. Similarly, it is essential for APIs or finished drug products manufacturing companies to ensure the safety of workers and the environment...
Things to be taken care while designing a cleanroom
Cleanrooms are essential to the manufacturing process for Lifesciences. The internationally accepted definition is "Cleanroom is a closed facility with a controlled flow of air, which is filtered and maintained free from external dust, microbes and contamination, as per certain standards...
Surrogate testing (OEL)– the Methodology to perform the OEL Validation
In my previous blog post, we focused on what OEL is and how it is categorized and a priority for containment solutions. In this blog post, we delve deeper to discuss how to perform the OEL validation process and the...