№ lp_2_1_35499
File format: docx
Character count: 2162
File size: 135 KB
Specification detailing required documents, processes, and compliance checks for suppliers submitting parts to ZAPI, classified by part type and production class.
Year:
2025
Organization:
ZAPI GROUP
Document type:
Technical Specification
Responsible:
F. Poggi
Revision history:
00 (14/03/2018), 01 (25/02/2020), 02 (08/09/2025)
Applicable to:
All ZAPI Suppliers
Categories:
Class 1, Class 2, Class 3, PCB, PCBA
Content:
Requirements for PPAP submission, including documentation, samples, compliance, and process controls
References:
ZPSF-2024-0020 Product Compliance, ZPSF-2017-0008 Supplier Quality Book
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2026
Organization:
TI Fluid Systems
Document Type:
Work Instruction
Scope:
Internal and external suppliers for manufacturing sites
Subject:
Production Part Approval Process (PPAP)
Related Standards:
AIAG PPAP, IATF 16949, APQP
Responsible:
Global Director Corporate Quality Systems
Target Audience:
TI Fluid Systems associates and suppliers
Submission Language:
English
Submission Levels:
1–5, Prototype
References:
CP-8-ALL-05, CF-8-ALL-0500, CF-8-ALL-0510, AIAG Manuals
Year:
2013
Region / City:
Nanisivik, Nunavut
Topic:
Spill Contingency Plan
Document Type:
Plan
Organization:
Department of National Defence, Defence Construction Canada
Author:
Stantec Consulting Ltd.
Target Audience:
Contractors, Facility Managers
Effective Period:
During construction and operation phases
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2018
Region / City:
United States
Subject:
Emission Standards, Engine Certification
Document Type:
Supporting Statement
Agency / Institution:
U.S. Environmental Protection Agency (EPA)
Author:
Certification and Compliance Division, Office of Transportation and Air Quality, Office of Air and Radiation
Target Audience:
Manufacturers, Environmental Regulatory Bodies
Effective Period:
Ongoing
Approval Date:
August 2018
Amendment Date:
N/A
Revision:
4
Revision date:
March 2022
Document type:
Supplier commitment and compliance statement
Organizations referenced:
CBRE; United Parcel Service (UPS)
Applicable jurisdiction:
United States
Subject matter:
Supplier personnel screening, site access, and safety requirements
Background check requirements:
Employment verification, criminal background checks, work authorization
Legal and regulatory references:
Immigration Reform and Control Act of 1986; OSHA requirements
Training requirements:
UPS-specific HSE training; CBRE expectation awareness training
Applicability:
Suppliers and subcontractors performing work on UPS sites on behalf of CBRE
Attachments:
Lockout Procedures Manual and related safety appendices
Contractual context:
Agreement between supplier and CBRE for services at UPS facilities
Year:
2018
Region / city:
Victoria, Australia
Theme:
Environmental Impact Assessment, Offshore Gas and Condensate Production
Document Type:
Environmental Plan Summary
Organization / institution:
Cooper Energy
Author:
Cooper Energy
Target Audience:
Stakeholders, Environmental Regulators, Industry Professionals
Effective Period:
Ongoing (Operations and Maintenance Phase)
Approval Date:
April 30, 2018
Revision Date:
April 30, 2018
Year:
2025
Region / City:
European Union
Topic:
Medical Devices
Document Type:
Application Form
Authoring Organization:
Medical Device Coordination Group (MDCG)
Target Audience:
Conformity assessment bodies
Period of Validity:
Ongoing
Approval Date:
January 2025
Amendment Date:
N/A
Document number:
DTCP-BWM-005
Revision:
3/2025
Issuing authority:
Wisconsin Department of Agriculture, Trade and Consumer Protection
Division:
Bureau of Weights and Measures
Jurisdiction:
State of Wisconsin
Legal basis:
Wisconsin Stat. §§ 15.04(1)(m), 93.06(1)(a), 93.07(2)
Public records status:
Subject to Wisconsin Public Records Law (Wis. Stat. §§ 19.31–19.39)
Document type:
Government complaint form
Scope:
Gas pump accuracy and fuel quality complaints
Submission methods:
Mail and email
Intended complainant:
Consumers
Confidentiality option:
Anonymous submission available
Contact office address:
Madison, Wisconsin
Version:
1.0.4
Note:
Region / City
Topic:
Software Installation
Document Type:
Revision History
Organization / Institution:
IVI Foundation
Target Audience:
Developers, System Administrators
Year:
2017
Region / City:
N/A
Topic:
LXI Conformance
Document Type:
Technical Specification
Organization / Institution:
LXI Consortium
Author:
LXI Consortium
Target Audience:
Developers, Engineers
Period of Validity:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Year:
2025
Region / city:
N/A
Subject:
LXI HiSLIP Extended Function
Document type:
Technical specification
Organization / institution:
LXI Consortium
Author:
LXI Consortium
Target audience:
Engineers, technical professionals, developers working with LXI standards
Effective period:
N/A
Approval date:
Sept 10, 2025
Amendment date:
N/A
Year:
2016
Region / City:
Not specified
Topic:
LXI Standards, VXI-11 Discovery Protocol
Document Type:
Technical Specification
Organization:
LXI Consortium
Author:
Not specified
Target Audience:
Industry professionals, engineers, and developers in LXI and VXI-11 technology
Validity Period:
Not specified
Approval Date:
8 November 2016
Amendment Date:
Not specified
Year:
2024
Region / City:
Not specified
Topic:
LXI API, API extended functionality
Document Type:
Technical Specification
Organization / Institution:
LXI Consortium
Author:
LXI Consortium
Target Audience:
Developers, Engineers, Technicians
Effective Period:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2025
Region / city:
Global
Topic:
LXI Specification, Interpretations and Clarifications
Document type:
Technical specification
Organization / institution:
LXI Consortium
Author:
LXI Consortium
Target audience:
Developers, engineers, and companies working with LXI devices
Effective period:
2023-2025
Approval date:
June 12, 2023
Revision date:
Feb 16, 2025
Year:
2023
Note:
Region / city
Topic:
Security Standards
Document type:
Technical Standard
Organization / institution:
LXI Consortium
Author:
LXI Consortium
Target audience:
Engineers, Technicians, Security Experts
Approval date:
January 26, 2023
Context description:
Technical standard outlining security features and compliance requirements for LXI systems.
Year:
2014
Region / City:
Geneva
Topic:
Revision of TGP/8, DUS Trial Design and Data Analysis
Document Type:
Draft Document
Organization / Institution:
International Union for the Protection of New Varieties of Plants (UPOV)
Author:
UPOV Office
Target Audience:
Technical Committees, Working Parties for Vegetables, Agricultural Crops, Fruit Crops, Ornamental Plants, and others involved in plant variety protection
Period of Validity:
Ongoing (as of 2014)
Approval Date:
May 27, 2014
Date of Changes:
N/A
Note:
Study Summary 1.1 Please provide a brief summary of the study in the table below. A complete description of the study with detailed information should be provided in the body of the protocol. For sections not applicable to the study, mark them as N/A. Study Title Study Design Primary Objective/Purpose Secondary Objective(s)/Purposes Research Intervention(s) ClinicalTrials.gov NCT # Study Population Sample Size Study Duration for individual subjects Study Specific Abbreviations/ Definitions
Background 3.1 Provide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how will it add to existing knowledge. :
this section should be limited to only information directly related to the research questions and objectives. Do not include your full dissertation proposal. 3.2 Describe any relevant preliminary data (e.g. pilot data).
Procedures Involved 5.1 Describe and explain the study design. 5.2 Please select the methods that will be employed in this study (select all that apply):
☐ Audio/Video Recording ☐ Psychophysiological Recording ☐ Behavioral Interventions ☐ Record Review - Educational ☐ Behavioral Observations and Experimentations ☐ Record Review - Employee ☐ Deception ☐ Record Review- Medical ☐ Focus Groups ☐ Record Review - Other ☐ Interviews ☐ Specimen Collection or Analysis ☐ Investigational Medical Device – (e.g. Medical Mobile Applications) ☐ Surveys and/or Questionnaires ☐Psychometric Testing ☐ Other Social-Behavioral Procedures Provide a description of all research procedures being performed and when they are performed. (Upload any surveys, questionnaires, interview scripts, focus group scripts, debriefing scripts, psychometric tests, stimulus materials, intervention manuals, and data collection forms on the Local Site Documents page in the IRB application.) 5.3 Describe the procedures or interventions that are going to be conducted as part of the research project, but that would have been conducted anyway, even if the research was not occurring (i.e. standard of care procedures, activities that would occur in a classroom). 5.4 Describe the procedures performed to lessen the probability or magnitude of risks of items selected in 5.2.5. 5 If accessing or collecting existing data, describe: The data that will be collected during the study (e.g. demographics, medical history, etc.). Attach the data capture sheet(s) on the Local Site Documents page in the IRB application. How the data will be obtained, including how you have the authority to access the data. The source or location of the data (e.g. USF Epic, TGH Epic, Hillsborough County School records, CANVAS records, publicly available databases, etc.). 5.6 If collecting and/or analyzing biological specimens, describe: How the biological specimens will be or have been collected. How the biological specimens will be stored. How long the biological specimens will be stored. How the biological specimens will be used. The laboratories that will be used. Whether the collected biological specimens will undergo genetic testing. If so, indicate if this study is part of a Genome Wide Association Study (GWAS) and whether the data will be forwarded to the NIH dbGaP. 5.7 If there are plans for long-term follow-up (once all research related procedures are complete), what data will be collected during this period.
Data and Specimen Storage for Future Research 6.1 If data or specimens will be banked for future research studies, describe where the data or specimens will be stored, how long it/they will b:
the process to request a release, approvals required for release, who can obtain data or specimens, and the data to be provided with specimens.