№ lp_1_12709
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The document is a request form for certification under various quality management systems (QMS) and regulatory assessments for medical device manufacturers.
Note:
Year
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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.
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]
Note:
Year
Region / City:
Canberra
Subject:
Female Genital Cutting (FGC), Clinical Guidelines, Healthcare
Document Type:
Clinical Guideline
Organization / Institution:
Canberra Health Services
Target Audience:
Healthcare staff (medical officers, nurse practitioners, registered nurses, midwives, allied health, students)
Contextual Description:
Clinical guideline outlining the management and prevention of female genital cutting (FGC) for healthcare providers at Canberra Health Services.
B. Tech (Computer and Communication Engineering) (applicable to students admitted from 2018 onwards)
Year:
2018
Region / City:
N/A
Subject:
Computer Science / Engineering
Document Type:
Academic Course Curriculum
Institution:
N/A
Author:
N/A
Target Audience:
Students of B.Tech program in Computer and Communication Engineering
Period of Application:
2018 and onwards
Date of Approval:
N/A
Date of Last Revision:
N/A
Note:
Year
Year:
1998
Region / city:
United States
Topic:
Repair and alteration services
Document type:
Contract Terms and Conditions
Agency / institution:
Federal Government
Author:
Not specified
Target audience:
Contractors, Government Agencies
Period of validity:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Year:
Not specified
Region / City:
Not specified
Subject:
Government equipment rental agreements
Document Type:
Contract
Agency / Institution:
Not specified
Author:
Not specified
Target Audience:
Government agencies
Period of validity:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified