Search results with tag "Conformity assessment"
Specification for the assessment of the life cycle ...
www.carbonconstruct.comLife cycle assessment – Requirements and guidelines, Clause 4.3.4.3 BS EN ISO/IEC 17050-1, Conformity assessment – Supplier’s declaration of conformity – Part 1: General requirements ISO/TS 14048:2002, Environmental management – Life cycle assessment – Data documentation format, Clause 5.2.2 IPCC 2006, Guidelines for National ...
Designation and notification of conformity assessment bodies
www.doks.nbog.euNBOG’s Best Practice Guide applicable for MDR, and IVDR 2017-1 NBOG BPG 2017-1 rev. 1 Page 1 of 16 Designation and notification of conformity assessment bodies
Accreditation for Conformity Assessment, Calibration and ...
www.thedti.gov.za4 No.29712 GOVERNMENT GAZEm, 16 MARCH 2007 Act No. 19,2006 ACCREDITATION FOR CONFORMITY ASSESSMENT, CALIBRATION AM) GOOD LABORATORY PRACTICE ACT, 2006 B E IT THEREFORE ENACTED by the Parliament of the Republic of South Africa, fOii0w~:- …
BUREAU OF INDIAN STANDARDS 16 Jun 2017 Subject: Draft …
bis.org.in2 BUREAU OF INDIAN STANDARDS 09 Jun 2017 Subject: Draft BIS (Conformity Assessment) Regulations, 2017 Draft BIS (Conformity Assessment) Regulations, 2017 …
Table of Contents - International Medical Device ...
www.imdrf.orgThis document should be read in conjunction with the GHTF document on Principles of Conformity Assessment for IVD medical devices that recommends conformity assessment
PERSONAL PROTECTIVE EQUIPMENT DIRECTIVE ( …
www.county-safety-services.comThe right to use the CE Marking may be obtained via Module A according to Conformity Assessment Procedures in Community Legislation. G 3.1.2 Category II
Guide to CE Marking & Radio Equipment Directive
www.elitetest.comThe focus of this document is to describe the CE Marking conformity assessment process for low power short range wireless devices.
SANAS Accreditation Toolkit
www.sanas.co.zaACCREDITATION TOOLKIT ©SANAS TERMINOLOGY CONTENTS A B C D E F G H I J K THE TERMINOLOGY USED IN THE WORLD OF ACCREDITATION • Conformity Assessment Bodies (CAB ...
ATEX IN SOUTH AFRICA by JG Auret, Explolabs …
www.explolabs.co.za3. THE ATEX APPROVAL PROCESS The flow diagram in Figure 2 describes the manner in which a manufacturer proves compliance with the EHSR’s and achieves CE marking for Ex equipment. Essentially, the steps are: Determine Group/Category of equipment Ł meet requirements for Conformity Assessment and
MEDICAL DEVICES: Guidance document
www.meddev.info- 3 - 1. PURPOSE AND PHILOSOPHY OF MEDICAL DEVICE CLASSIFICATION It is not feasible economically nor justifiable in practice to subject all medical devices to the most rigorous conformity assessment procedures
IECEE OPERATIONAL DOCUMENT - IEC System of …
www.iecee.orgIECEE OD-2025-A IECEE OPERATIONAL DOCUMENT INTERNATIONAL ELECTROTECHNICAL COMMISSION PRICE CODE ZZ IEC System of Conformity Assessment Schemes for Electrotechnical
EQUIVALENCE AND ACCEPTANCE BETWEEN ELECTRONIC …
www.intertek.comA: The agreements will allow the designated products to enter the Mexican market with either a certificate of compliance with the official Mexican standard (NOM) or with a document or certificate issued according to the technical regulations and conformity assessment followed in the U.S. and
Guide to Method Validation for Quantitative …
www.inab.iePS15 Guide to Method Validation for Quantitative Analysis in Chemical Testing Laboratories Issue 4 February 2016 Page 5 of 27 ISO/IEC 17043:2010 Conformity assessment -- General requirements for proficiency testing [14] [15] BIPM, IEC, IFCC, ISO, IUPAC, IUPAP, OIML: Guide to the expression of uncertainty in measurement, …
INTERNATIONAL ISO/IEC STANDARD 17024
www.ihf-fih.orgConformity assessment — General requirements for bodies operating certification of persons. 1. Scope . This International Standard contains principles and requirements for a body certifying persons against specific requirements, and includes the development and maintenance of a certification scheme for persons.
SOP-1 Accreditation Procedure-General Form-Rev 1
www.pjlabs.comAccreditation Procedure Accreditation Procedure First Issue: 02/05 Revision 1.12 SOP-1 Revised: 2/17 Page 1 of 17 PJLA offers third-party accreditation services to Conformity Assessment Bodies (i.e. Testing
PLACEMENT OF MEDICAL DEVICES ON THE MALAYSIAN …
mdb.gov.myPLACEMENT OF MEDICAL DEVICES ON THE MALAYSIAN MARKET Conformity assessment and placement on the market Medical device regulatory system is intended to ensure protection of public health and safety.
Schedule of Accreditation - slab.lk
slab.lkPage 02 of 02 Deputy Director (Accreditation) Sri Lanka Accreditation Board for Conformity Assessment Colombo, Sri Lanka SI. No. Type/ Field of
GHTF SG1 - Summary Technical Documentation (STED) for ...
www.imdrf.orgconformity assessment activities. This technical documentation subset is intended to be in a consistent, summarised or abridged form, with sufficient detail to allow the
MEDICAL DEVICES Guidance document Classification of ...
www.meddev.info4 1. PURPOSE AND PHILOSOPHY OF MEDICAL DEVICE CLASSIFICATION It is not feasible economically nor justifiable in practice to subject all medical devices to the most rigorous conformity assessment procedures available.
Conformity Assessment of Medical Devices Under The New …
www.mdrivdr.comScope: MDR Article 1 and 2 MDR Conformity Assessment: MHRA* (UK Competent Authority) MDR Annex IX, X, XI Class I, IIa, IIb, III and Custom Made Devices Must Know What requirements need to be met for a conformity assessment? Summary *Medicines and Healthcare Products Agency
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