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6th January 2009, 03:31 PM
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Process Audits for Medical Devices
Small Medical Device instrument manufacturer. Just passed our Audit but the Auditor missed items that I thought we would be written up. We ended up with one minor and a few observations. The minor was for doc control (mixed revisions) of documents in a Device History Record. I looked back on the Internal Audits and found nine incidents of minors written for doc control. Training was also an issue, with people selectively picking and creating training records at the last second.The internal audit corrective actions were not effective for doc control and we missed being bagged for training. Granted I'm not complaining but this was a gift that needs to be fixed. My opinion is we should double our auditing efforts in a few of these lacking areas and add some sort of process type audit for random checking. Any suggestions would be appreciated. Great Thanks
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6th January 2009, 04:39 PM
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Re: Process Audits for Medical Device
You are thinking exactly what I would be thinking.
One benefit if having outsiders come to view our management systems is that we can also learn something about ourselves by observation, if we pay attention. It sounds like you have doen that. By all means, use what you have observed as focus points to make your audit master plan.
When I do audits of whatever type, I audit all kinds of elements. Document control is always there, as are records and usually training. I'll draw a sample of records from the process being audited. This way I can learn two things:
If it's local to a group or system-wide
If it's just a temporary glitch or a systemic looking problem
Based on the above, when it comes time to audit that element (training, for example) I can begin with an idea of what to put in my audit plan. I might even decide that an unscheduled audit is called for to do that, if waiting invites too big a risk.
I hope this helps!
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Thanks to Jennifer Kirley for your informative Post and/or Attachment!
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6th January 2009, 05:13 PM
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Re: Process Audits for Medical Device
I hope your management takes the view that getting away with stuff is bad, not good.
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Thanks to MIREGMGR for your informative Post and/or Attachment!
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6th January 2009, 05:29 PM
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Re: Process Audits for Medical Device
Did the auditor look at process planning, controls, feedback etc as specified in the GHTF guidance? It seems odd that the non-conformances are for the old auditor favourites of doc control & training.
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6th January 2009, 05:47 PM
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Re: Process Audits for Medical Device
That's another story - sometimes they like hearing themselves talk.
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6th January 2009, 05:51 PM
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Re: Process Audits for Medical Device
An unscheduled random audit is definitly in the plan.
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6th January 2009, 05:53 PM
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Re: Process Audits for Medical Device
We will definitely fix it.
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7th January 2009, 02:52 AM
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Re: Process Audits for Medical Devices
Sorry, in that type of a sceanrio, I would look to improve the quality of the internal auditing and auditors and not merely increase the number of auditors.
Few ideas -
1. You could also explore the idea of self auditing the own department by the dept representatives before the Internal Auditor steps in.
2. You could also have the Layered Process Audits (LPA) to have the involvement of one and all.
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