ISO 9000 is a series of internationally recognized standards that have been developed and published by the International Organization for Standardization (ISO) to guide organizations in establishing and maintaining effective quality management systems (QMS). These standards are based on universally accepted principles of quality assurance and management. The ISO 9000 family aims to help organizations … Read more
Clean area classification is a system used to categorize environments based on the level of cleanliness required for specific activities or processes. It is a critical aspect of industries such as pharmaceuticals, biotechnology, electronics manufacturing, and healthcare, where the presence of contaminants can have significant consequences on product quality and safety. The classification standards are … Read more
Pharmaceutical sieves are essential tools in the pharmaceutical industry, used to separate and classify pharmaceutical materials based on particle size. These sieves are crucial in quality control, formulation development, and pharmaceutical manufacturing. Here’s a detailed note on pharmaceutical sieves and the standards that govern their use: Pharmaceutical Sieves Pharmaceutical sieves are precision instruments for performing … Read more
