Validation Protocol Execution Tips

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  • 8/9/2019 Validation Protocol Execution Tips

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    Validation Protocol Execution Tips Top 10

    1. Ensure that the protocol has been written from an approved design document. Theres

    no point in developing tests from an unapproved FS (Functional Specification) or DS

    (Design Specification) if the design is going to change. Your protocol needs to reflect

    what is in your approved design document.

    2. The person who is developing the protocol needs to understand what needs to be

    tested.

    3. Ensure that you have sufficient time before you run the protocol to dry run it.

    4. Treat the dry run as a real run, document all of your test results like you would the real

    run (Youll be surprised what you find!)

    5. If you have time, get an independent person to review your protocol, they will spot

    things you will never see.

    6. Start the execution at the start of your day when you are fresh, not at the end when you

    are rushing and want to go home.

    7. Ensure that all of the prerequisites have been performed before execution

    8. Have deviation and discrepancy forms at hand to write them up as you go along (You

    will forget the details if you dont)

    9. Understand what is the difference between a deviation or a discrepancy (Or whatever

    terminology your company uses)

    10. Attach any evidence you deem important

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    QUALIFICATION & VALIDATION

    Qualification is a process of assurance that the specific system, premises or equipmentare able to achieve the predetermined acceptance criteria to confirm the attributes what it

    purports to do.

    Validation is establishing a documented evidence to provide a high degree of assurancethat a specific system, process or facility will consistently produce a product meeting its

    predetermined specifications and quality attributes.

    Qualification is documented evidence that a specific equipment, facility or system isfit/ready for intended use.

    Validation is documenting that the way equipment, facility or system used will result in

    product meeting its predetermined specifications and quality attributes.

    Things are qualified: equipments, systems etc.

    Process/Procedures (the way we use things) are validated.

    Before you do validation on a process, you have to be sure that the equipment has passed

    qualification

    Globaly....yes, you can say like that, but...perhaps is better to say..calibration is one of

    condition to make qualification, as well as qualification is one of condition to makevalidation.

    Also, don't forget..this is important and very clarify (from the first post)..

    ''Things are qualified: equipments, systems etc.

    Process/Procedures (the way we use things) are validated.

    Before you do validation on a process, you have to be sure that the equipment has passed

    qualification.''