Regulatory Open Forum

 View Only
  • 1.  Thoughts on skipping PQ

    This message was posted by a user wishing to remain anonymous
    Posted 14-Dec-2022 09:45
    This message was posted by a user wishing to remain anonymous

    Hi,
    I recently received a request about the possibility to skip process PQ as our customers are in desperate need of our product and instead carry out 100% visual inspection of the products that are shipped. The idea is then to carry out the process PQ runs at a later stage when our customers have been able to stockpile a bit. The reason this comes up is that our PQ runs will be very extensive.
    My initial thought is that this is off the table because I can't find anything that suggests we can make an exception to doing a full process validation.

    Do you have any experience in dealing with a similar question, alternatively if you have knowledge of how to handle this type of question from a QA/RA perspective? Any other possible approaches to handle this request instead of doing the 100% visual inspection?

    A little context: Works for a manufacturer of a class 1 medical device that is intended to be packed together with a drug as a combination product at our customer and then sold on the US and Japanese market.

    Thank you in advance.


  • 2.  RE: Thoughts on skipping PQ

    Posted 26-Dec-2022 18:18
    This is a duplicated post. See responses HERE

    ------------------------------
    Ajit Basrur
    Worcester MA
    United States
    ------------------------------