№ files_lp_3_process_7_087497
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The document outlines the required materials and procedures for the submission of a Quality Management System (QMS) for review by SIM QSTFNMI/DI, including specific submission requirements, peer reviews, internal audits, and other supporting documentation.
Note:
Year
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2023
Region / City:
Global
Topic:
Mobile Technology, Telecommunications
Document Type:
Industry Specification
Organization / Institution:
GSM Association
Author:
GSM Association
Target Audience:
Telecom industry professionals, device manufacturers, network operators
Effective Period:
Not specified
Approval Date:
March 25, 2023
Amendment Date:
Not specified
Year:
2023
Region / City:
Global
Topic:
Mobile network technology
Document Type:
Industry Specification
Organization / Institution:
GSM Association
Author:
GSM Association
Target Audience:
Industry professionals, device manufacturers, network operators
Period of Validity:
Ongoing
Approval Date:
March 2023
Date of Changes:
Not specified
Note:
Year
Document type:
Template
Year:
2023-2024
Region / City:
Not specified
Topic:
Quality Management System, Metrology
Document Type:
Report
Author:
Not specified
Target Audience:
Quality Management Professionals, Metrology Experts
Period of Validity:
January 1, 2023 to June 30, 2024
Date of Approval:
Not specified
Date of Changes:
Not specified
Major Changes:
Significant organizational and staffing changes, modifications to CMC delivery, changes in Quality Management System
Key Issues:
Inconsistent results with published CMCs, customer complaints, nonconformities
Status of CMCs:
Greyed-out CMCs, progress updates
Date of Last Management Review:
Not specified
Summary of Changes:
Major updates to the Quality Management System, affecting the validity of CMCs
Contact Information:
Name, Role/Title, email address
Report Type:
Annual Report, Quality Management System Overview
Year:
2026
Region / City:
Kent, UK
Theme:
Social Housing, Accessible Housing, Charity Retail, Digital Connectivity, Corporate Parenting
Document Type:
Meeting Minutes / Report
Organization:
Kent County Council (KCC), Various Charities and Local Authorities
Author:
Various Speakers and Contributors
Target Audience:
Local Authorities, Social Housing Providers, Charity Representatives, Government Departments
Action Period:
Ongoing
Approval Date:
2026
Amendment Date:
2026
Year:
2025
Date:
05/05/2025
Time:
8:30 AM
Location:
HFH - Detroit - Simulation Center
City:
Detroit
Country:
United States
Institution:
Henry Ford Health
Document Type:
Continuing Medical Education Course Information
Medical Field:
Point of Care Ultrasound
Topic:
Bedside ultrasound assessment for critically ill patients
Educational Format:
Live course with didactic teaching and hands-on simulation
Maximum Credit:
4.00 AMA PRA Category 1 Credits™
Accrediting Organization:
Accreditation Council for Continuing Medical Education
Course Director:
Danielle J. Bastien
Co-Director:
Madison Osentoski, PA-C
Faculty:
Andrew Bissonette, MD; Daniel Jourdan, MD-Resident; Jia Liu, MD-Fellow; Kevin Wang, DO-Fellow
CME Reviewer:
Crystal M Gyiraszin, MS
CME Specialist:
Denise Brooks, MBA
Target Audience:
Faculty
Organizing Institution:
Henry Ford Health
Disclosure Status:
No relevant financial relationships disclosed
Year:
2023
Organization:
SIM (Serving In Mission)
Document Type:
Guideline / Guidebook
Audience:
Regional Directors, Entity Directors, healthcare workers, sending office recruiters
Purpose:
To provide foundational principles for planning, implementing, and evaluating healthcare ministries
Scope:
Global SIM healthcare ministries
Core Topics:
Prayer, biblical grounding, mission alignment, partnerships, best practices, sustainability, governance, creativity
References:
SIM Ministry Principles and Practice document, Healthcare and the Mission of God by Dr. Paul Hudson
Key Components:
10 foundational principles, self-evaluation tool, integration with other ministries, long-term relationship building
Language:
English
Note:
Year
Year:
2025
Region / City:
Not specified
Subject:
Business information management, client onboarding, and compliance
Document Type:
Business policy and procedure manual
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Business clients, tax agents, BAS agents
Period of validity:
Ongoing
Approval Date:
6th May 2025
Date of Amendments:
Not specified
Note:
Year
Subject:
Quality Management System for tax practitioners
Document type:
Guide
Organization / Institution:
Tax Practitioners Board
Target audience:
Tax practitioners
Note:
Year
Topic:
Quality Management System
Document Type:
Template
Year:
2024
Region / City:
United States
Subject:
Safety Assurance Evaluation
Document Type:
Instructional Reference
Organization:
FAA
Author:
Daniel J. Elgas
Target Audience:
Approval holders in the aviation industry
Period of Validity:
Ongoing
Approval Date:
05/03/2024
Amendment Date:
N/A
Year:
2023
Region / city:
Birmingham
Topic:
Quality Management System in Clinical Research
Document Type:
Standard Operating Procedure (SOP)
Organization / Institution:
University of Birmingham
Author:
Clinical Research Compliance Team (CRCT)
Target Audience:
Research teams, Clinical Trials Units, QMS managers
Effective Date:
[Not specified]
Date of Approval:
[Not specified]
Date of Changes:
[Not specified]
Year:
2025
Region / City:
Brussels, Belgium
Topic:
Quality Management System Compliance
Document Type:
Report
Organization:
ETICS
Author:
ETICS
Target Audience:
Inspectors, ETICS-CIG-Inspection Scheme Members
Validity Period:
Not specified
Approval Date:
April 2025
Date of Amendments:
Not specified
Supersedes:
OD CIG 023 Appendix 2 – December 2020
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:
2010
Region / city:
[not specified]
Topic:
Medical Devices, Quality Management Systems
Document Type:
Declaration
Organization / Institution:
[Company name]
Author:
[Company representative]
Target Audience:
Health regulatory authorities
Period of validity:
[not specified]
Date of approval:
[not specified]
Date of amendments:
[not specified]
Year:
2024
Document Type:
Form Template / Instructional Reference
Revision:
0
Effective Date:
05/03/2024
Approval:
Daniel J. Elgas, Director, Policy and Standards Division, AIR-600
Objective:
Confirm communication of safety information and training within organization
Evaluation Tool:
Data Collection Tool (DCT) – Safety Promotion
Regulatory References:
§ 5.23, § 5.91, § 5.93, § 5.97(c-d), AC21-58
Year:
2024
Region / City:
Not specified
Subject:
Safety Risk Management (SRM)
Document Type:
Template
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Approval holders, SMS teams
Effective Period:
Not specified
Approval Date:
05/03/2024
Modification Date:
Not specified
Year:
2024
Region / City:
Not specified
Subject:
Safety policy and performance evaluation
Document Type:
Instructional Guide
Organization:
AIR-600, Policy and Standards Division
Author:
Daniel J. Elgas
Target Audience:
Approval holders, SMS team members, evaluators
Period of Validity:
Not specified
Approval Date:
05/03/2024
Date of Last Changes:
Not specified
Note:
Revision History
Rev:
0
Description of Change:
Original Release
Effective Date:
05/03/24
Approval:
/s/ Daniel J. Elgas
Date:
05/03/2024
Approval Holder:
SMS
Verification Dates:
SMS Follow Up Verification Dates (if applicable):
REGULATORY REQUIREMENT:
§ 5.91
REFERENCE:
AC21-58, paragraph 2.6.1