by Clean Rooms Ability | Oct 28, 2022 | Blog
IMPLEMENTING GOOD MANUFACTURING PRACTICES: PHARMACEUTICAL GMPS Blog Implementing Good Manufacturing Practices: Pharmaceutical GMPs *Contains Nonbinding Recommendations Good Manufacturing Practices are a set of guidelines and principles that ensure the quality and...
by Clean Rooms Ability | Sep 6, 2022 | Blog
DO I NEED A LAB, CONTROLLED ENVIRONMENT OR A CLEAN ROOM? Laboratory- Little to no environmental controlA laboratory is often used to describe a facility where research, experiments, and testing can occur. Sometimes laboratories do not need to follow rigorous...
by Clean Rooms Ability | Sep 6, 2022 | Blog
For a pharmacy compounder to mix prescriptions safely and properly according to legal regulations, a compounding cleanroom is required. The cleanroom is where you will use and house specific equipment such as a laminar airflow workstation (LAFW) and a compounding...
by Clean Rooms Ability | Sep 6, 2022 | Blog
More than a room that is clean or a controlled environment, according to the ISO standard 14644-1 clean room definition, a clean room is defined as: “A room in which the concentration of airborne particles is controlled, and which is constructed and used in a manner...
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