Hello Friends, Recently we have implemented SAP System (ERP), for that in QMS aspect I have focused on Change management, Risk management,...
Hello Everyone, A Non conformance is raised for not updating the approved supplier list during Internal Audit. hence, it is found that system is...
Is it recommendable / acceptable to have individual manual for QMS and Business process (if willing to have a manual) I may feel it should be...
Thank you @John C. Abnet
Hello friends, I work in a manufacturing company which is located at Sharjah - UAE, we have utilizing the resources like Chillers and Air...
Thank you brother for the detailed clarification and also I have a doubt on, what if incase of only "mould validation". what should I do? For...
Dear Brothers & Sisters, Greeting of the Day.. I need your assistance regarding Process Validation - Injection Moulding Process (Special Process...
Thank you brothers and sisters for sharing your opinion. Its really helpful improve my perspective and understanding...
Hello Haddad9921, As you said, "do we need to keep record of us considering the items a - j?".. yes as stated in the clause No.8.3.2.j - "the...
Shall we consider either it may or may not affect product conformity, if so shall we raise NC if not conforms to the requirement but conforms to...
Can any one share me the interaction matrix of standards with processes for the purpose to cover audit area...mainly ISO 9001:2015 ISO...
can you tell me that any one of your customer (OEM) deals with On road vehicles and also share your process flow, so that I can understand about...
Then in the sense that it is a process design, right? ISO 9001 2015, clause no: 8.3, doesn't applicable to out organization ?
Hello Everyone, We are the manufacturers of Detergent powders, liquids and soaps as well, what I felt doubt with the requirement of ISO 9001:2015...
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