№ lp_1_2_53937
File format: docx
Character count: 3205
File size: 71 KB
This document outlines the terms and conditions for the use of the combined ILAC MRA mark for conformity assessment bodies accredited by Norwegian Accreditation (NA), including testing laboratories, calibration laboratories, and inspection bodies.
Note:
Year
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.
The file will be delivered to the email address provided at checkout within 12 hours.
Don’t have cryptocurrency yet?
You can still complete your purchase in a few minutes:- Buy Crypto in a trusted app (Coinbase, Kraken, Cash App or any similar service).
- In the app, tap Send.
- Select network, paste our wallet address.
- Send the exact amount shown above.
The final amount may vary slightly depending on the payment method.
The file will be sent to the email address provided at checkout within 24 hours.
The product description is provided for reference. Actual content and formatting may differ slightly.
Document type:
Agreement
Parties:
MRA Systems, LLC (Middle River Aerostructure Systems) and Supplier
Industry:
Aerospace manufacturing
Subject:
Delegated supplier product release and quality responsibilities
Applicable standards:
AS9117, AS13001, AS13100, SS1182, MRAS M1000, MRAS M1002
Delegated role:
Delegated Quality Representative (DQR)
Governing organization:
MRA Systems, LLC
Scope:
Material and services purchased by MRAS
Status:
Contractual document upon signature
Revision history:
Initial release; subsequent revisions A and B
Approval authorities:
MRAS Quality, MRAS Supplier Quality, Supplier management
Geographic context:
United States
Year:
Not specified
Region / City:
Not specified
Topic:
Medical Reimbursement Allowance, Direct Deposit
Document Type:
Form
Organization:
Plumbers and Pipefitters Medical Fund
Author:
Not specified
Target Audience:
Participants in the Plumbers and Pipefitters Medical Fund
Effective Period:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Description:
This document is a form for participants in the Plumbers and Pipefitters Medical Fund to authorize automatic direct deposit for Medical Reimbursement Allowance (MRA) benefits.
Note:
Year
Subject:
Portland Cement Concrete Pavement Conformity
Document Type:
Contract Specification
Target Audience:
Contractors, Engineers
Year:
2017
Region / City:
European Union
Theme:
Medical Device Regulation
Document Type:
Regulatory Document
Organization / Institution:
Medical Device Coordination Group (MDCG)
Target Audience:
National Authorities, Notified Bodies, Conformity Assessment Bodies
Period of Validity:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2017
Region / City:
N/A
Theme:
Medical Device Regulation
Document Type:
Fee List
Organization / Institution:
Notified Body XXXX
Target Audience:
Manufacturers of medical devices
Period of Validity:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Note:
Year
Topic:
Transportation Air Quality Conformity
Document Type:
Checklist
Year:
[Month Year]
Region / city:
[General location information]
Topic:
Air Quality Conformity Analysis
Document Type:
Report
Target Audience:
[Not specified]
Period of Effect:
[Not specified]
Approval Date:
[Not specified]
Date of Modifications:
[Not specified]
Revision date:
January 2023
Document type:
Instructions and sample cover letter
Jurisdiction:
California
Region:
United States
Primary agency:
California Department of Transportation
Federal agency:
Federal Highway Administration
Subject area:
Transportation conformity and air quality
Regulatory framework:
40 CFR Part 93
Pollutants referenced:
Ozone, CO, PM10, PM2.5, NO2
Related processes:
NEPA Assignment under 23 USC 327
Intended use:
Project-level conformity determination correspondence
Audience:
Transportation and air quality professionals
Note:
Year
Contextual description:
A document certifying the conformity of a vehicle with the ADR regulations for the carriage of dangerous goods.
Year:
2023
Region / City:
EU
Subject:
Medical Devices
Document Type:
Regulatory Document
Author:
Medical Device Coordination Group (MDCG)
Target Audience:
National Authorities, Conformity Assessment Bodies, Medical Device Manufacturers
Applicable Period:
N/A
Approval Date:
N/A
Date of Amendments:
N/A
Note:
Year
Topic:
Road and Bridge Construction Specifications
Document Type:
Standard Provision
Organ / Institution:
Construction Engineering Services Branch
Target Audience:
Engineers, Contractors
Year:
2021
Month:
July
Document type:
MDCG guidance document
Issuing group:
Medical Device Coordination Group (MDCG)
Regulatory framework:
Regulation (EU) 2017/746
Related regulation:
Regulation (EU) 2017/745
Subject:
Applied-for scope of designation and notification of a Conformity Assessment Body
Field:
In vitro diagnostic medical devices
Geographical scope:
European Union
Legal status:
Non-binding guidance
Endorsement:
Endorsed by the Medical Device Coordination Group
Standard referenced:
IO-Link Interface and System Specification V1.1.5
Note:
Standard referenced
IO Device Description V1.1.5
Additional specifications:
IO-Link Common Profile Specification V1.2.1
Issuing organization:
Manufacturer of IO-Link devices
MD version:
V1.1.5
MD release date:
October 2025
Relevant test specification:
V1.1.5, June 2025
Conformity evidence:
Test report(s)
Authorization:
Authorized signatory required
Intended use:
Declaration of conformity for IO-Link devices
Applicable system:
IO-Link
Source type:
Technical compliance declaration
Year:
2025
Country:
India
Regulatory framework:
Central Motor Vehicle Rules
Standard type:
Automotive industry standard
Subject area:
Vehicle emissions testing and compliance
Test procedure:
Worldwide harmonized Light vehicle Test Procedure (WLTP)
Vehicle categories:
M1, M2, N1
Maximum permissible mass:
3500 kg GVW
Scope:
Type approval, Conformity of Production (COP), In-Service Conformity (ISC)
Related UN regulations:
UN GTR No. 15 Amendment 6, UN GTR No. 19 Amendment 3
Issuing body:
Automotive Industry Standards Committee
Publishing organization:
Automotive Research Association of India
Supervising authority:
Ministry of Road Transport and Highways, Government of India
Date of publication:
January 2025
Date of hosting on website:
16 December 2025
Comment deadline:
14 January 2026
Testing areas covered:
Type I to Type V tests, WLTC, RDE, OBD, evaporative emissions, durability
Source type:
Regulatory technical standard
Prepared by:
Office of Non-clinical and Clinical Compliance, Pharmaceutical and Medical Devices Agency
Organization:
Pharmaceutical and Medical Devices Agency
Country:
Japan
Date of preparation:
January 26, 2017
Version:
1.0
Subject area:
Medical devices regulation
Topic:
Non-clinical studies
Document type:
Regulatory guidance
Inspection type:
Document-based conformity inspection
Legal basis:
Law on Securing Quality, Efficacy and Safety of Products Including Pharmaceuticals and Medical Devices
Target materials:
Supporting data and documents for approval applications
Scope:
Non-clinical studies of medical devices
Intended users:
Applicants for medical device approval and inspection personnel
Year:
2024
Note:
Region / city
Topic:
IO-Link Master conformity
Contextual description:
A document certifying the conformity of an IO-Link Master product with specified standards, including possible exceptions.