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gayathrisatheesh
Ours is a product manufacturing co. and I am looking for details and preparations required in terms of process, audits, documentation, production for ISO 9001 2008/2009
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Ours is a product manufacturing co. and iam looking for details and prepartions required in terms of process, audits, documentation, production for ISO 9001 2008/2009
Here is some of my advice:Ours is a product manufacturing co. and I am looking for details and preparations required in terms of process, audits, documentation, production for ISO 9001 2008/2009
Ours is a product manufacturing co. and I am looking for details and preparations required in terms of process, audits, documentation, production for ISO 9001 2008/2009
I am looking for input on selecting a webinar for training for transition from 2000 to ISO 9001:2008. Has any one had any good experiences? All input appreciated.
Here is some of my advice:
DO NOT buy a 'canned', off-the-shelf quality management system because it will not work and will create more headaches in the future. Every effective QMS is particular and taylored to its organization's needs.
Like Andy said, get yourself copies of the standards (ISO 9000, ISO 9001 & ISO 9004). Reading them will help you understand the requirements, interpretations, definitions, etc. They will also be a handy reference during imprementation and future audits.
Like Harry suggested, invest time into reading through the forums and the attached files. You will find many 'what if', 'how to', 'what about' scenarios along with valuable insight and interpretations. You will also find many sample procedures, forms, probably even some quality manuals (if not, I'll post one). Look at the formats and identify what format makes most sense to you (ease of reading, editing, maintenance, distribution, retrieval, etc). Also look at the contents to see examples of how one requirement can be addressed in more than one way. Again, select something that makes sense and could be taylored to your organization's needs.
Last but not least, consider your customers' requirements when developing the QMS. Some of them can be integrated as bast-practices or GMP's, others are very specific. Regardless, they have to be reviewed and addressed (see clause 7.2).
I would be happy to look at and try to answer to more specific questions if you have any.
Heavy going, though, particularly for the newby. Unless you like reading a dictionary.Without ISO 9000:2005 you do not have the whole picture.