IQ Protocol

Installation Qualification is defined as, establishing by objective evidence that all key aspects of the process equipment and ancillary system installation adhere to the manufacturer’s approved specification and that the recommendations of the supplier of the equipment are suitably considered.

Comment List

  • PharmaState Academy
    08/07/2019

    what are the testing requirements for incoming raw materials such as vials, syringes, needles, gowns etc. Can we use vendor C of A for these consumable components? Also, what are the testing requirements for the incoming solvents and reference standards? Please, advise. Thanks

  • PharmaState Academy
    08/07/2019

    Great information all around on this website.

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