Guest
My name is *** and I am the Quality Assistant of our *** Manager, ***.
I will be investigating the implementation of the ISO 27001 with a group of colleagues and will report to ***accordingly.
First I’d like to thank you upfront for sharing your expertise and information below to hopefully help us decide to purchase this toolkit.
We are very interested in your toolkit below yet some topics crossed our minds of which we are curious to know before purchasing.
Since we are already certified for ISO 13485 I was wondering how this could be of advantage to us in implemented the ISO 27001 standard.
Therefore these questions raised:
1 - For instance, would it be sufficient for us to adjust certain procedures we already have because of this? Besides creating new ones that are required of course.
2 - Is integrating ISO 27001 into our Quality Management System possible?
3 - Does a gap analysis exist between ISO 13485 and ISO 27001 and if so, has it already been made?
4 - Is this kind of information also addressed extensively in your toolkit?
What do most people find most difficult to implement
What is the best way to be adopted in an attempt to establish an effective PIMS based on ISO 27001 and ISO 27018 and perhaps consider ISO 27701
Assign ownership and accountabilities for strategic, aggregated, dynamic risks
Dear Dejan,
We started working with Conformio, and first of all: I think it’s very useful! Thank you for it.
I just have a question: I noticed all document templates have a block with “code, version, date of version etc” and later on a block with “change history”. This doesn’t make sense to me, since we are already using Conformio as a document management system where these things are already properly documented for each file. Can I remove these in my documents?
I am asking this because I want to make our documents as short as possible, so our employees actually do read them (the more unnecessary info the more distraction and I’m afraid they will scroll rather than really read). Therefore, I would also like to skip the “reference documents”. Is that allowed too?
Thanks for your advice.