Equipment Qualification

Equipment Qualification

Equipment Qualification is the final series of inspections and tests to ensure that critical requirements necessary for related product quality are satisfied and that documents and procedures necessary to properly operate and maintain the system are in place. The VMP fiat the actions that all persons involved in equipment validation projects must comply with. The Equipment Validation Plan (VP) may often be designed to include more than one piece of equipment. The list of equipment will be attached to the plan.

Each of these items will have its own flow of documentation; typically:

VP - URS – FS / DS - DQ - VRA - IQ - OQ - PQ

All regulatory required documentation must be carefully prepared, with statements framed to prevent questionable and incorrect interpretations of the purpose of the statement. In addition there are quite separate requirements specified by the regulatory authorities. Documents presented to regulatory bodies during inspections that goes wrong to satisfy these requirements, indicate to the regulator a deficiency of care and faithfulness on the part of the organization. The exact opposite to what is necessary.

To overcome these problems we introduced our self in pharmaceutical business with downright set of documentation for equipment qualification venture. We extend following documents which are crucial for equipment qualification program.