Document control procedure manual

This process description provides a standard process for document control and records management. Document control and records management are addressed in 10 CFR 50 Appendix B as follows: VI. Document Control Measures shall be established to control the issuance of documents, such as instructions, procedures, and drawings, including changes . V. PROCEDURE 1. Creating New Documents a. SOP’s must use the standard format template and include a standard header on each page. b. Each SOP must have: i. Descriptive document title (e.g. Document Control) ii. Unique document number (e.g. SOP) iii. Effective date iv. Revision number2 v. Document history section, used for describing changes. vi.  · Procedure for Control of Documented Information. preteshbiswas Uncategorized Decem. Ma. 10 Minutes. 1. SCOPE. To ensure that the documented information. including all documents of internal external origin, is controlled with respect to approval, distribution, change, etc. www.doorway.ruted Reading Time: 9 mins.

The document control process applies to Policies, Manuals, Standard Operating Procedures, Job Aids, Templates and Supporting Documents (e.g. quality system controlled documents) that are governed by the TQMS quality management system (QMS). Exit Criteria Document is ready as input to 'Document Review and Approval' procedure i.e. the author submits the changed document for review. Outputs and Records The changed document Checkout information created. Reviewing and approving the documents Section Name Section details Procedure Id Document Control Process v Document and Records. Policy # Title. Last Updated: QDRMI Documents and Records Policy: Mar Quality Manual Procedure Template. Mar QDRMId. Standard Operating Procedure Template. Mar QDRMIe. Orientation Training Checklist Template. Mar

Document Control Procedure for Manual Electronic Document Management System The document control procedure of any company describes the control mechanisms to ensure that master documents are controlled with regards to their approval, revision, issue level, distribution and use. Quality Manual Specification () for the Quality Management System Specification Document () Stating Requirements Objective Evidence Data () Supporting The Existence or Verity of Something Output •Document approval •Process control •Continual improvement •Document changes •Record control How •Documented information. Documentation Control Process Office of the President Page 1 Rev. 3 PURPOSE The purpose of this process is to ensure that the correct version of documentation is available at all times. The procedure covers the review and control of all documentation in the Quality Management System. This includes: Quality Manual Quality Policy.