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Training others to perform internal audits
On completion of this course will I be able to train others to perform internal audits? -
Gap analysis feedback
How can I design a gap analysis feedback? -
Cumplir con el contexto de la organización
Hola soy el RD de mi empresa, pero apenas nos vamos a certificar, tengo una duda en el formato del Entorno de la Organización, el asesor que nos ayuda en la certificación me pasó un formato de Entorno de la Organización, pero hay un formato, o sólo basta con cumplir el punto 4 de la norma? -
Objectives, risks and opportunities and the HR department
I want guidelines on how to draft quality objectives, Risks and Opportunities for the HR department -
Riesgos en ISO 9001, cambios versión 2015 y activos importantes
Me gustaría saber que aspecto hay que tomar en cuenta para la realización de un matriz de riesgo en un empresa de alimentos,cuales fueron los cambios mas radicales de la norma ISO 9001 2015, Y cual seria el activo mas importante de una organización. -
Context: a controlled document?
Please help me decide whether to keep ISO 9001 context as a controlled document, to be distributed to all the relevant stakeholders or not. -
Design controls
I have found your site very helpful and have purchased a few items as a result. I have experience managing an ISO 9001 facility and transitioning from 2008 to 2015. My current issues are in the design and development section, because my experience has been in service industry where we were able to disregard that clause. I'm in a new position where I'm working to implement ISO 9001 for the first time and don't understand how to fully implement that clause. -
Writing a production instruction manual guide
Can you help me write a production instruction manual guide to ISO 9001? Is there an example that describes the criteria I must adhere to? -
Validation vs Verification
I and my team are making an ATV (sae Baja vehicle) and we supposed to submit our design validation plan can you tell me what are the key features that differentiate validation from verification -
Withdrawing documents
A document was not being used (format). Hence it was withdrawn. During internal audit I (MR) was questioned, how I had withdrawn. What is the evidence, who approved it etc. I had done it on the verbal communication by the engineer working in the process. How is to be done actually?