№ files_lp_3_process_7_064640
File format: docx
Character count: 4841
File size: 567 KB
Year:
2015
Region / City:
Geneva, Switzerland
Topic:
Change management in Quality Management Systems
Document Type:
Paper
Organization / Institution:
International Organization for Standardization
Author:
ISO 9001:2015 Committee
Target Audience:
Organizations implementing ISO 9001:2015
Period of Validity:
Ongoing
Approval Date:
2015
Revision Date:
Not specified
Description:
A paper outlining how changes should be planned, controlled, and implemented within the Quality Management System as per ISO 9001:2015.
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2025
Region / City:
United States
Topic:
Medicare Advantage, CCO, Dual Eligible, FBDE, Healthcare Integration
Document Type:
Guidance Document
Agency / Organization:
Centers for Medicare & Medicaid Services (CMS), Oregon Health Authority (OHA)
Author:
Centers for Medicare & Medicaid Services (CMS), Oregon Health Authority (OHA)
Target Audience:
Coordinated Care Organizations (CCOs), Medicare Advantage Plans, Health Providers
Effective Period:
2025
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2014
Region / City:
Bouie
Subject:
Technology
Document Type:
Educational Plan
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Students
Period of Validity:
3/10/14-3/14/14
Approval Date:
Not specified
Date of Changes:
Not specified
Context:
Educational plan outlining weekly learning objectives and tasks for students working with Microsoft Word and PowerPoint, focusing on flyer design, clip art, word art, shapes, and effects.
Year:
2015
Region / City:
Kabul, Afghanistan
Subject:
Violence against Women, Legal Framework, Mediation, Court Adjudication
Document Type:
Report
Organization:
United Nations Assistance Mission in Afghanistan (UNAMA), United Nations Office of the High Commissioner for Human Rights (OHCHR)
Author:
UNAMA, OHCHR
Target Audience:
Policymakers, Legal Professionals, Human Rights Advocates, International Organizations
Period of Effect:
2014-2015
Date of Approval:
April 2015
Date of Amendments:
Not specified
Year:
2015
Region / City:
Geneva, Switzerland
Topic:
Quality Management System
Document Type:
Guideline
Organization:
International Organization for Standardization (ISO)
Author:
ISO
Target Audience:
Organizations implementing ISO 9001:2015
Effective Period:
Ongoing
Approval Date:
Not specified
Revision Date:
Not specified
The document outlines the procedures for addressing changes within the Quality Management System as outlined in ISO 9001:
2015, emphasizing how such changes can impact processes, resources, and risk management in organizations.
Year:
Not specified
Region / City:
Not specified
Subject:
Self-reflection, Equality, Personal Growth
Document Type:
Personal Statement
Institution:
Not specified
Author:
Not specified
Target Audience:
Admission committees, potentially universities
Validity Period:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2015
Region / city:
Vernier, Geneva, Switzerland
Topic:
Quality Management System (QMS)
Document Type:
Implementation Guidance
Organization / Institution:
International Organization for Standardization (ISO)
Author:
ISO/TC 176/SC 2
Target Audience:
Organizations using ISO 9001, National Standards Bodies, Accreditation Bodies, Certification Bodies, Trainers and Consultants
Period of validity:
Ongoing during transition period
Approval Date:
2015
Date of Changes:
Not specified
This document provides guidelines for organizations transitioning from ISO 9001:
2008 to ISO 9001:2015, focusing on the revision process, user groups, and implementation steps.
Year:
2015
Scope:
Quality Management System (QMS) implementation
Document Type:
Guide
Organization:
ISO
Target Audience:
Consultants, Organizations seeking ISO 9001 certification
Regulatory Requirements:
ISO 9001:2015
Industry Standards:
ISO 9001:2015
Key Personnel:
Consultants, Management
Process:
QMS implementation, internal audits, ISO registration
Training:
QMS training, internal audits
Certification:
ISO 9001 Certification
Phase:
Initial Assessment, Planning, Development and Implementation, Concluding, Pre-assessment, Registrar Audit and Registration, Post Registration and Surveillance Audits
This document outlines the phases and steps for implementing an ISO 9001:
2015 Quality Management System (QMS), focusing on the assessment, planning, development, and certification process.
Year:
2015
Region / City:
Geneva, Switzerland
Topic:
ISO 9001:2015 Revision
Document Type:
FAQ
Organization:
International Organization for Standardization
Author:
International Organization for Standardization
Target Audience:
ISO 9001 users and experts
Period of validity:
Not specified
Approval Date:
Not specified
Date of changes:
Not specified
This document is a collection of frequently asked questions related to the revision of ISO 9001:
2015, providing insights into the updates and changes in the standard, including topics like risk-based thinking and changes in the documentation requirements.
Year:
2015
Region / City:
Geneva, Switzerland
Topic:
Quality Management
Document Type:
Standard
Organization / Institution:
International Organization for Standardization
Author:
ISO
Target Audience:
Organizations implementing or following ISO 9001:2015
Effective Period:
Ongoing
Approval Date:
Not specified
Date of Changes:
Not specified
The document describes the process approach in ISO 9001:
2015, including how organizations can use it to integrate their processes and improve the management system.
Year:
2015
Region / city:
Vernier, Geneva, Switzerland
Topic:
ISO 9001:2015, Quality Management Systems
Document type:
Guidance
Organization / institution:
International Organization for Standardization (ISO)
Author:
Not specified
Target audience:
Organizations implementing or maintaining a quality management system
Effective period:
Not specified
Approval date:
Not specified
Date of amendments:
Not specified
The document provides guidance on the documentation requirements for ISO 9001:
2015, offering insights into the scope, maintenance, and retention of documented information within a quality management system.
Year:
2015
Region / City:
Geneva, Switzerland
Topic:
Quality Management System
Document Type:
Guideline
Organization:
International Organization for Standardization (ISO)
Author:
ISO
Target Audience:
Organizations implementing ISO 9001:2015
Effective Period:
Ongoing
Approval Date:
Not specified
Revision Date:
Not specified
The document outlines the procedures for addressing changes within the Quality Management System as outlined in ISO 9001:
2015, emphasizing how such changes can impact processes, resources, and risk management in organizations.
Year:
2015
Region / City:
Not specified
Subject:
Quality Management System, ISO 9001:2015 Certification
Document Type:
Self-assessment, Quality Management System Compliance Evaluation
Organ / Institution:
Not specified
Author:
Not specified
Target Audience:
Organizations seeking ISO 9001:2015 certification
Validity Period:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
This document serves as a self-assessment tool for organizations to evaluate their readiness for ISO 9001:
2015 Quality Management System certification.
Organization:
PRECISION/EXPEDITED
Address:
28482 Airoso Street, Rancho Mission Viejo, CA 92675
Standard:
ISO 9001:2015
Document Type:
Quality Manual
System:
Quality Management System (QMS)
Methodology:
Plan-Do-Check-Act (PDCA)
Scope:
Quality management system processes and controls
Leadership:
William R. Towery, President
Policy:
Quality Policy focused on customer satisfaction and continual improvement
Structure:
Sections aligned with ISO 9001:2015 clauses (Context, Leadership, Planning, Support, Operation, Performance Evaluation, Improvement)
Application:
Precision parts manufacturing and expedited services
Source Type:
Corporate quality management documentation
Corporate quality management manual outlining the structure, policies, processes, and responsibilities of an ISO 9001:
2015-compliant quality management system for precision parts manufacturing and expedited services.
Year:
2022
Region / City:
Global
Topic:
ISO 9001:2015, ISO 22301:2019, ISO/IEC 27001:2022 Management Systems Audit
Document Type:
Audit Report
Organization:
MSECB
Author:
MSECB Audit Team
Target Audience:
Company management, certification authorities
Period of Validity:
May 12, 2022 - May 15, 2022
Approval Date:
May 15, 2022
Date of Changes:
N/A
Audit Scope:
Certification for ISO 9001:2015, ISO 22301:2019, ISO/IEC 27001:2022
Audit Objectives:
To verify conformance with ISO 9001:2015, ISO 22301:2019, ISO/IEC 27001:2022 requirements
Audit Methodology:
Process-based audit focusing on significant aspects and risks
Audit Findings:
No major nonconformities, one minor nonconformity found
Conclusion:
Recommendation for certification
Year:
202X
Region / City:
Not specified
Subject:
Information Security Management
Document Type:
Surveillance Plan
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Not specified
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Surveillance plan for ISO/IEC 27001:
2013, ISO/IEC 27018:2019, ISO 9001:2015, detailing audit activities and control objectives to be reviewed.
Year:
2015
Region / city:
Geneva, Switzerland
Topic:
ISO 9001:2008 to ISO 9001:2015 correlation matrices
Document type:
ISO Standard
Organization:
International Organization for Standardization (ISO)
Author:
ISO Technical Committee
Target audience:
Quality management professionals, ISO auditors, organizations implementing ISO 9001
Validity period:
Ongoing
Approval date:
2015
Amendment date:
N/A
This document is a correlation matrix comparing the clauses of ISO 9001:
2008 and ISO 9001:2015 to highlight differences in structure, terminology, and content.
Year:
2015
Region / City:
N/A
Topic:
ISO 9001:2015 compliance
Document type:
Checklist
Organization:
N/A
Author:
N/A
Target audience:
Organizations implementing ISO 9001:2015
Validity period:
N/A
Approval date:
N/A
Amendment date:
N/A
A checklist to evaluate compliance with ISO 9001:
2015 Clauses 4 to 10.
Year:
2013
Region / city:
Switzerland
Subject:
Standardization, ISO standards
Document type:
Technical document draft
Organization / institution:
ISO
Author:
ISO Technical Committee
Target audience:
Professionals in standardization and technical committees
Effective period:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Year:
2021
Region / City:
National
Field:
Medical
Document Type:
Assessment Forms
Organization:
National Accreditation Board for Testing and Calibration Laboratories (NABL)
Author:
NA
Target Audience:
Laboratories, Assessor Teams, Medical Imaging
Period of Validity:
Not specified
Date of Approval:
16-Feb-2021
Amendment Date:
13-Jul-2023
The document outlines assessment forms and checklists used by the NABL for the accreditation of laboratories in accordance with ISO 15189:
2012 standards, including various schedules and witness reports for medical testing.
Year:
2023
Note:
Region / City
Theme:
Accreditation, Laboratory Assessment
Document Type:
Assessment Forms and Checklists
Organization / Institution:
National Accreditation Board for Testing and Calibration Laboratories (NABL)
Target Audience:
Laboratories seeking accreditation
Description:
A set of forms and checklists used for assessing laboratories based on the ISO 15189:2022 standard.