GMP Annex 1 2022 Update Breakdown: Part 2
In 2017, GMP released a draft update to Annex 1, which received a lot of feedback.
October 26, 2022
In 2017, GMP released a draft update to Annex 1, which received a lot of feedback.
A cleanroom classification basically tells you how clean a cleanroom is. While we typically consider cleanrooms
The European Union (EU) Good Manufacturing Practice (GMP) for Medicinal Products for Human and Veterinary Use
It is no mystery that cleanrooms need to be, well, clean. From the surfaces and tools
If you use compressed gasses in your cleanroom, ISO 8573 is an important set of guidelines
If you know us, then you know that clean air and water is our passion in
Welcome to the age of the internet! Pharma 4.0 is the International Society for Pharmaceutical Engineering’s (ISPE) version
Did you know we start to mitigate risk in our lives as early as 6 months
If you are relatively new to the cleanroom world, you’ve probably heard the word “reverse osmosis”
If you are working with a pharmaceutical or semiconductor manufacturing cleanroom, you most likely have seen
What is the biggest villain in the contamination control and cleanroom world? Particles. Contamination. This contamination
Everyone with a cleanroom could use a particle counter, right? But which particle counter is right
Does it matter what kind of particle exists in your cleanroom? Yes, it does! Two types
It’s no secret that COVID-19 has drastically impacted the world around us. Throughout August 2021, the
Good Manufacturing Practices (GMPs – sometimes referred to as Current Good Manufacturing Practices or CGMPs) are federal
What Is Cleanroom Paper? [Case Study] Do you use print-outs in your cleanroom? What kind of
https://youtu.be/vSS_uJlrvvk If you’re working for a company already using a cleanroom, you’re well aware of the
Particle counters do just that: they count particles. They are used in cleanrooms to count and size the
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