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Activities: Regulatory Medical Devices Pharmaceutical

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    What is ISO 8 cleanroom classification? Each cleanroom class is denoted by a maximum concentration of particles per cubic meter or cubic foot of air. ISO 8 is the second lowest cleanroom classification
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    Integrity testing of HEPA filters: A practical approach Filtering the air in aseptic process areas is critical to maintaining the cleanliness of the production environment. Jesus Casas provides tips to ensure HEPA filters are fit...
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    The importance of growth promotion testing Given the critical nature of microbiological quality tests which are employed to ensure that pharmaceutical products are safe for human use, it is in turn essential to...
  4. Nortek Air Solutions CleanSpace relaunches SERVICOR for modular cleanrooms Nortek Air Solutions CleanSpace shared with Cleanroom Technology how SERVICOR for modular cleanrooms, complies with ANNEX 1 requirements, as it was relaunched to meet industry...
  5. BES completes Terumo Aortic cleanroom build started pre-covid Cleanroom construction expert has finished the 2,400 sqm manufacturing facility with cGMP cleanrooms for the medical device manufacturer

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