ISO 9001 Required Forms & Records (4.2.4)
What is the difference between a form and a record?
- A form is a place to record data.
- A form with data is now a record.
- A record provides objective evidence of data, activities, etc., and in ISO 9001 it helps to establish evidence of conformance to QMS requirements.
- Organizations must retain records which are legible, readily identifiable and retrievable.
- The 9000 Store offers a complete set of forms & Records
ISO 9001 only requires six (6) procedures, but it identifies twenty-six (26) types of records:
ISO 9001:2008 Required Forms
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Quality management systems - Guidelines for quality plans
- 5.6.1 Management Reviews
- 6.2.2 Competence, awareness and training
- 7.1 Planning of product realization
- 7.2.2 Review of requirements
- 7.3.1 Design planning output
- 7.3.2 Design and development inputs
- 7.3.3 Design and development output
- 7.3.4 Design and development review
- 7.3.5 Design and development verification
- 7.3.6 Design and development validation
- 7.3.7 Design and development changes
- 7.4.1 Purchasing process
- 7.5.1 Control of production and service provision
- 7.5.2 Validation of processes for production and service provision
- 7.5.3 Identification and traceability
- 7.5.4 Customer property
- 7.6 Control of monitoring and measurement equipment
- 8.2.2 Internal audit
- 8.2.4 Monitoring and measurement of product
- 8.3 Control of nonconforming product
- 8.4 Analysis of data
- 8.5.2 Corrective action
- 8.5.3 Preventive action
The 9000 Store offers a complete set of forms & Records