№ lp_1_2_57191
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This explanatory document outlines the criteria for self-assessment of conformity assessment schemes and provides guidance for conformity assessment bodies (CABs) applying for accreditation.
Year:
2018
Region / city:
Netherlands
Topic:
Conformity assessment schemes
Document type:
Explanatory note
Organization:
Dutch Accreditation Council (RvA)
Author:
Dutch Accreditation Council (RvA)
Target audience:
Conformity assessment bodies (CABs) applying for accreditation
Validity period:
Ongoing
Approval date:
20 February 2018
Date of last change:
20 February 2018
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The product description is provided for reference. Actual content and formatting may differ slightly.
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.
Author:
Gregory Dubois-Felsmann
Organization:
Large Synoptic Survey Telescope (LSST) Project
Document identifier:
LSE-82
Related documents:
LSE-81; LPM-17; LSE-29; LSE-30; LDM-138; LDM-141
Document type:
Technical explanation report
Subject area:
Astronomy data management and survey science
Revision date:
August 15, 2011
Revision history:
Versions 1, 1.1, 1.2
Survey duration referenced:
10-year survey
Primary topics:
science estimates; camera specifications; survey cadence; data management sizing; storage and network requirements
Intended use context:
LSST data management and system design
Technical source type:
Project internal technical documentation
Year:
2025
Region / City:
Atlanta, Georgia
Subject:
National Healthcare Safety Network (NHSN) Surveillance Changes
Document Type:
Program Change Explanation
Organization:
Centers for Disease Control and Prevention (CDC), Division of Healthcare Quality Promotion
Author:
Paula Farrell
Target Audience:
Healthcare professionals involved in data collection for NHSN
Effective Period:
Until 06/30/2025
Approval Date:
May 12, 2025
Amendment Date:
N/A
Context:
The document describes changes to a data collection instrument used for healthcare facility surveillance as part of the NHSN system, detailing revisions to data collection and formatting guidelines.
Note:
Year
City:
Englewood
Document Type:
Rent Adjustment Notice
Department:
Building Department
Note:
Year
Topic:
Allied Health, Mental Health Services
Document Type:
Informational Text
Organization / Institution:
LTW Clinic
Target Audience:
General public, patients, healthcare professionals
Note:
Year
Topic:
Health Care
Document Type:
Explanation of Benefits