Projects in the CAPA system

Hello! We would like to start using our CAPA system to track some of our bigger projects, so that we can keep track of due dates, etc.
My question is, for a project such as revising procedures and processes to meet an updated ISO standard, would you consider that a corrective or preventive action? We are an ISO 13485 medical device manufacturer.
Thank you!

Either your fixing something that's broke or your improving something so it won't break. or to make it better.

The reason for your dilemma is that you're trying to put a round peg into a square hole. What you need is some form of project management software, be it a dedicated software package or a well-crafted spreadsheet. In my own view, corrective and preventive actions should be kept separate as they are in entirely different categories, but to try and shoehorn project management into the system is entirely inappropriate.

Jim Wynne said:

The reason for your dilemma is that you're trying to put a round peg into a square hole. What you need is some form of project management software, be it a dedicated software package or a well-crafted spreadsheet. In my own view, corrective and preventive actions should be kept separate as they are in entirely different categories, but to try and shoehorn project management into the system is entirely inappropriate.

Click to expand...

Yes, I agree, but we are a small company with limited resources. I can also create a project plan and then execute and document as a report, but I wanted to put it into the QMS somehow. Thanks for the input!

I had a COO that directed a company I used to work for to use an APQP project if we were going to be spending $5000 or more. He wanted to ensure the cross functional team was reviewing the project at every phase. We even used the APQP process to decide and then launch our office upgrades.

You are following your QMS> Likely in your quality manual you state you review regulatory requirements and keep them up to date. These would be routine QMS changes.

Add the item to your quality plan as a task. Open a QMS Change, title it "Updates to QMS documents, forms and procedures to align with ISO XXX," rev all the items with the required changes, review old/new risks and release them. Train, etc. Done. An auditor is not likely to look in your CAPA log to see if you are compliant with the ISO standard; they will start with your Quality Manual and go through your QMS overall.

Ed Panek said:

Open a CN...

Click to expand...

What is a CN?