ISO 9001: 2015 Quality Management System Full Documentation

ISO 9001 Quality management systems - Requirements 

Our Services:
We provide documentation design services for ISO 9001 Quality management System which includes the following listed documents: Quality Manual and Mandatory procedures for ISO certification. We provide both standard and customized documentation design services.

As per the Client requirements, We input the provided organization business and process specific information into the standard documents and customize them for ready to use/ implement.

List of Documented Information to be Maintained (Mandatory Requirement) - ISO 9001:2015

High level Documents:
Scope of the QMS (clause 4.3)
Documented information necessary to support the operation of processes to the extent determined by the Organization  (clause 4.4) 
The quality policy (clause 5.2) 
The quality objectives (clause 6.2) 
Documented information requirements of clause 7.5

List of Documented Information to be Maintained (Non-mandatory Requirement) - ISO 9001:2015

Low Level Documents
Examples documents:
Organization charts
Process maps, process flow charts and/or process descriptions
Procedures  (Technical/ QA Procedures)
Work and/or test instructions  
Specifications  
Documents containing internal communications
Production schedules
Approved supplier lists
Test and inspection plans
Quality plans
Quality manuals
Strategic plans
Forms

List of Documents to be Retained (Mandatory Requirement)- ISO 9001:2015

Documented information to the extent necessary to have confidence that the processes are being carried out as planned (clause 4.4).
Monitoring and measuring equipment calibration records* (clause 7.1.5.1)
Records of training, skills, experience and qualifications (clause 7.2)
Product/service requirements review records (clause 8.2.3.2)
Record about design and development outputs review* (clause 8.3.2)
Records about design and development inputs* (clause 8.3.3)
Records of design and development controls* (clause 8.3.4)
Records of design and development outputs *(clause 8.3.5)
Design and development changes records* (clause 8.3.6)
Characteristics of product to be produced and service to be provided (clause 8.5.1)
Records about customer property (clause 8.5.3)
Production/service provision change control records (clause 8.5.6)
Record of conformity of product/service with acceptance criteria (clause 8.6)
Record of nonconforming outputs (clause 8.7.2)
Monitoring and measurement results (clause 9.1.1)
Internal audit program (clause 9.2)
Results of internal audits (clause 9.2)
Results of the management review (clause 9.3)
Results of corrective actions (clause 10.1)

Please contact us for the complete documentation package of ISO 9001:2015 QMS for implementation.  

For Queries/ Orders please contact: qaqc.estores@gmail.com
Web: www.qaqcdocumentstores.com

No comments

Powered by Blogger.