Documentation for Pharma Industries

Documentation for Pharma, Food and Dairy Industries

Documentation IQ, DQ, OQ – We as MECHZEAL achieve total compliance to industry and regulatory standards for equipment and components
 

PRINCIPLE:

Documentation is an integral part of good manufacturing practices. It defines a system of information and control so that risks so inherent in misinterpretation and/or error in oral communication are minimized.
 

Mechzeal is having OBJECTIVES OF DOCUMENTS and submitting along with each projects of Water generation, storage, distribution system as well utility piping.

 

  • Design qualification is defined as a verification process on the design to meet particular requirements relating to the quality of pharmaceuticals/ dairy and manufacturing practices.

 

  • Installation Qualification is a documented process that verifies that all aspects of facility, utilities and equipment that affect product quality adhere to the approved design specifications, and that the piece of equipment or instrument has been properly delivered.

 

  • Operational Qualification, or OQ, is an essential process during the development of equipment often used by customers. OQ can simply be defined as a series of tests which ensure that equipment and its sub-systems will operate within their specified limits consistently and dependably.

 

  • Manuals: SOP, Operation procedure and Maintenance procedure shall be covered under manuals provided to customer at the time of project handing over and training.