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Internal audit schedule
I am working on a new internal audit schedule, now I was advised to start a 3 year cycle, auditing the most important processes first.
Nice, for me all processes feel important. There certainly is an kind of standard perception on the importance of processes / ISO13485 paragraphs.
Are you able to help out and guide me in this one?
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Writing quality SOP for work infrastructure
How to write quality SOP for work infrastructure? -
Medical Device File
Is Medical Device File (ISO 13485:2016 requirement 4.2.3) called Technical File in MDD 93/42/EEC, is it the same file?
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FDA
Our company is ISO 13485:2016 certified. We have a new customer who wants us to manufacture and pack hearing aid. As you know FDA doesn't require 510K for Hearing Aid, but the customer wants us to register with FDA.
Without 510K what will be our company's responsibilities for the product if we decide to register with FDA.
Please advise.Thank you for your help in advance
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SOP for Control of Nonconforming Product/Proces
We currently have no process for RMAs, but we do have an SOP for Control of Nonconforming Product/Proces. Typically, do you see these as separate SOPs, or are they usually combined? I'm relatively new to ISO 13485 and 9001 and am not really sure how to go about writing the procedure for this. -
Seperation of the ISO13485/MDR toolkit.
I received mdr ISO13485 templates and would like to know how to seperate the folder structure between ISO13485 templates and MDR? I have multiple products and desire one QMS.
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When is there a need to open and handle a complaint?
Hello,
first of all thank you, that you offer this service and even free of charge!
I have more or less a simple question:
Does a complaint only begin when a company receives a complaint from a customer ( oral, written or electronic) OR also when a customer reports a case to a service hotline, e.g. if the medical device is not working properly and the service team can fix the problem - but there might be a problem with the device in general that needs to be investigated?
In the latter case, the company itself would initiate the complaint, but I wonder if this is even necessary because it was not officially reported by a customer?I hope if it is clearly to understand what I mean.. :)
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All documents required by QMS for ISO13485
I would like to ask if the list of internal documents priced for 9.9 include list of all documents required by QMS for ISO13485:206?
I need only list including tittles, for study pourpose.