1.1 - Quality Management System (QMS) Overview equipment repair and investigate if this may

and investigate if this may result in a risk of illness or injury

or other extraneous material

and shall have adequate space for the orderly placement of equipment and materials to prevent mix-ups and contamination

There shall be separate or defined areas necessary to prevent contamination or mix-ups during receipt

1.1 - Quality Management System (QMS) Overview equipment repair and investigate if this mayTo ensure pharmaceutical products are fit for their intended use, and do not place patients at risk due to inadequate safety, quality or efficacy, there must be a comprehensively designed and correctly implemented Pharmaceutical Quality System incorporating Good Manufacturing Practice and Quality Risk Management. The attainment of this quality objective is the responsibility of senior management