Current Good Manufacturing Practice (cGMP) is about building quality into all working procedures so that the risk of making mistakes is reduced to a minimum and we maintain consistency in our products and processes. It is a regulatory requirement. For the purpose of cGMPs the definition of ‘quality’ is that a product must be ‘fit for its intended purpose’. This module details the training and validation requirements that must be completed by operators working in technical services.
Hand decontamination is the single most important means of preventing the spread of infection; this is a key part of GMP.
The vast majority of cross infection within a clean room area is the result of the transfer of organisms from person to person by the hands of staff.
Touch contamination is the most common source of clean room contamination and occurs via the operators. Therefore, proper hand washing and disinfection are key components to eliminate this type of cross contamination. This procedure is used when entering and exiting a clean room environment and ensures that staff do not contaminate the clean room environment, work stations or products.
Effective hand decontamination can significantly reduce both cross transmission and cross infection rates
