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Quality Systems and SOPs for Manufacturing GMP Products

Quality Systems are made up of Standard Operating Procedures (SOPs) and policies, but there
is more to the picture than just the individual documents. A well-organized quality system also defines the relationships between procedures. In any organization, almost every process is dependent on or has an impact on another.  While each SOP may define a select set of tasks, the more important concept is to make sure all the tasks are integrated so there are few chances for overlaps or redundancies. This reduces the chance of errors being made.  Keeping a focus on systems integration improves the efficiency of the whole organization.

Prevention Rather Than Reaction
Following SOPs

Maintaining quality systems prevents problems and mistakes. Prevention is more economical than reacting after a problem occurs. If the processes are properly defined, SOPs provide guidelines and processes for employees to follow to reduce the possibility of human error. Well-written SOPs reduce organizational dependence upon individual and institutional knowledge.

Financial success is a way of measuring the results of improving quality. As improvements are made to processes, the Standard Operating Procedures are updated, and employees can implement the new processes in tandem. Less waste and greater productivity are the consequences that lead to greater profits.  Quality improvements also increase product reliability. Your customers know what to expect from your
business each time.

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