Eliminating contaminants in an area of high GMP cleanliness

Published: 13-Jul-2023 Featured companies: Vileda Professional CE
Containment

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Need to deliver your facility a Next Level Clean, sustainably? Does the GMP Annex1 revision present new SOP’s challenges with regards to contamination control in your facility?

If so, read Vileda’s article on “Efficient elimination of contaminants in the area of high GMP cleanliness classes, for pharmaceuticals and medical devices” now!

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  1. Identifying and preventing contaminant leakage from your cleanroom A common solution to machinery contamination in a cleanroom is to build a cleanroom within a cleanroom using partitions or curtains, to isolate the machine. Chris Lindlar from Subzero Engineering discusses how a comprehensive simulation technique to analyse and predict the distribution of contaminants in the environment to prevent contaminant leakage can be implemented
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  3. ANSI/NSF 49:2019 vs EN 12469:2001: How do they compare? There are variations in biosafety cabinet standards, but how do their instructions differ, and should you be aiming higher? Ivan Kaliman from Zwei Ingenieria explains
  4. Glove testing systems: ensuring the highest levels of safety Barrier systems such as isolators or RABS play a fundamental role in the protection of people and products in pharmaceutical production. Only tenths of a millimetre thick, gloves are the most crucial interface in these hermetically sealed units, writes Matthias Angelmaier, Product Manager, Barrier Systems at Syntegon Technology
  5. Guarding cleanroom cleanliness: How Dycem helped Touchlight prevent contamination UK-based Touchlight is taking a revolutionary approach to DNA production and has secured a pivotal role in supporting the development of genetic medicine and advanced therapies. As a Contract Development and Manufacturing Organization (CDMO) working with over 100 biotech and pharmaceutical companies, Touchlight is committed to providing state-of-the-art facilities to meet the needs of their customers

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