admin

ISO 29990 :2010 – Learning Services For Non-Formal Education What is ISO 29990? ISO 29990 sets out the criteria for a Quality Management System standard for providers of education and training services. ISO 29990 provides a unified standard for learning service providers, including corporations, vocational institutions, and life-long learning centres, around the globe. It promotes […]

ISO 11607 – PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES What is ISO 11607? The process of developing and constructing a packaging system for terminally sterilized medical devices is a convoluted and pressing endeavor. The definitive nature of the medical device, the intended sterilization methods, the intended use, expiration date, transport, and storage all influence the

ISO 14155 – GOOD CLINICAL PRACTICES What is ISO 14155? The International Organization for Standardization (ISO) publishes the ISO standard for Good clinical practices (GCP) for the design, conduct, recording, and reporting of clinical studies with medical devices. Conducting your clinical studies according to GCP is important not only to collect good quality data under

ISO 22716 – GOOD MANUFACTURING PRACTICES FOR COSMETICS What is ISO 22716 ? ISO 22716 is an international standard of good manufacturing practices (GMP) for the cosmetics manufacturing industry and describes the basic principles of applying GMP in a facility that produces finished cosmetic products. This guideline offers organized and practical advice on the management

ISO 22483:2020 – TOURISM QUALITY MANAGEMENT SYSTEM What is ISO 22483? The ISO 22483 standard, originally designed by the British Standards Institute (BSI), was reconsidered by the International Standards Organization (ISO) and re-published as an international standard. The last update of this standard was made in 2020. This standard creates quality requirements and recommendations for

ISO 11011:2013 – COMPRESSED AIR – ENERGY EFICIENCY What is ISO 11011? ISO 11011:2013 sets requirements for conducting and reporting the results of a compressed air system assessment that considers the entire system, from energy inputs to the work performed as the result of these inputs. ISO 11011:2013 considers compressed air systems as three functional

HIGG FEM – HIGG FACILITY ENVIRONMENTAL MODULE What is HIGG FEM? The Higg Facility Environmental Module (Higg FEM) is a sustainability assessment tool that standardizes how facilities measure and evaluate their environmental performance, year over year. The Higg FEM informs brands, retailers, and manufacturers about the environmental sustainability performance of their individual facilities, so they

Current Good Manufacturing Practices (cGMP) What is cGMP? In the United State, Current Good Manufacturing Practices known as CGMP, refer to legislation that falls under the purview of the U.S. Food and Drug Administration (FDA). These laws ensure that all pharmaceuticals and most food and beverage, cosmetic, and dietary supplement companies follow industry and best