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In this video, learn what are Documents & Records "Must-Have" in clause 4.0 up to 6.0 of ISO 9001:2015 Quality Management System as well as Clause 7.5 Documented Information. Feel free to share your comments below and any additional inputs on this topic that we can all share and apply in our respective ISO 9001:2015 management system documents and records control. Thank you for watching. You may watch more related videos 🤍agfconsultinggroup430 Heard about ISO 9001:2015? If you haven't, no worries! AGF has you covered! Here's a quick video on ISO 9001:2015 in a nutshell. Find out how it works and how it can work for you and your company in this link below: 🤍youtu.be/qSVqDNOkOTo Learn about the the Plan-Do-Check-Act (PDCA) Cycle, the pertinent clauses for the requirements on ISO 9001:2015 and most importantly know how to meet and exceed your client's expectations while continuously improving your processes! What more could you ask for? Brought to you only by the best in the business on ISO Consultancy, AGF Consulting Group-PH! Need help on ISO Consultancy? Looking for a training partner? Choose AGF now! #thinkAGF. Watch more related videos 🤍AGF Consulting Group
If you still think, in this day and age, that a document controller is a person, you don’t understand ISO and have no clue on how to use technology.
Hey guys, what's QMR? Thank you.
how do you do that?
Your video is good. HOWEVER,
. Why ISO needs to complicate everything?
They need to be straightforward, with simplicity of words and presentation. Simple systems will be adopted.
Hi, thanks for your work. It's really very helpful :)
Are you really sure that 7.5.2.c requires us to have in all documented information a strict information who and when approved it? You don't have to have all documentation in word or pdf, you can have them in some tool where it's not possible to add such information but as long as you can prove that it was approved before publication (you know who approved it and when) it should be ok.
For example, process maps that we have in a separate cloud base tool, where we have a approval workflow for each process. We have clear evidence who and when aprroved it to be publish, relevant version of a process. We don't have to have information on a process map who and when approved it (of course we can, but I don't think that it's mandatory).
Another example, we can imagine that we're creating a training in Power Point, save it to PDF and put in some tool that automatically send invitations to employees who should perform the training and monitor who did it. Before we will put the training to the tool, we're gather feedback from our colleagues and Manager and implement their suggestions. We have evidence in email box that it was revised and approved, so we don't have to have information on a first slide who and when approved it (of course we can, but I don't think that it's mandatory).
What is your perspective on that?
Is Quality manual mandatory
What are the mandatory documents
I had watched so many videos for same...yet I find your description most amazing...keep up the good work man!
Very informative and well explained. It helps us to easily understand QMS.
Excellent video
Let us know what are you key take away(s) in this short video. Thank you for sharing your inputs, insights and comments. What you share here will probably create positive impact more than you could ever know. Together, we can all learn and advance, as one. youtube.com/results?search_query=%23thinkagf #ThinkAGF
Learn ISO 9001:2015 in a nutshell. Click link below to watch:
youtu.be/qSVqDNOkOTo youtu.be/qSVqDNOkOTo
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