The LIST of the SNAS METHODICAL GUIDELINES for ACCREDITATION

General
Identification Title Effective from PDF Extra Note
MSA-02 SNAS logo and marks 01/17 Click for open file    
MSA-04 Procedure for the accreditation 01/17 Click for open file    
MSA-05 Requirements for SNAS assessors and experts 01/17 Click for open file    
MSA-06 Responsibility of SNAS and CAB 08/16 Click for open file    
MSA-07 EA requirements for the accreditation of flexible scopes (EA-2/15) 05/17   Info  (effectiveness of the Slovak translation)
Laboratories
Identification Title Effective from PDF Extra Note
MSA-L/01 Field and scope of accreditation of laboratories 01/15 Click for open file    
MSA-L/02 Use of proficiency testing as a tool for accreditation in testing (EA-3/04) 08/13   Info  
MSA-L/04 Guidelines on the reporting of compliance with specification (ILAC-G8: 03/2009) 01/17   Info  (effectiveness of the Slovak translation)
MSA-L/08 Interlaboratory comparison in calibration laboratories 08/13 Click for open file    
MSA-L/11 Guidelines on the expression of uncertainty in quantitative testing (EA-4/16: 2013) 02/17   Info  (effectiveness of the Slovak translation)
MSA-L/12 Expression of the uncertainty of measurement in calibration (EA-4/02) 01/17   Info  (effectiveness of the Slovak translation)
MSA-L/14 Determination of the level and freqency of proficiency testing participation (EA-4/18: 2010) 02/17   Info  
Inspection bodies
Identification Title Effective from PDF Extra Note
MSA-I/01 Accreditation scope and scope specification of accreditation of inspection bodies 02/17 Click for open file    
MSA-I/02 Guidance on the application of ISO/IEC 17020:2012 (ILAC-P15:06/2014) 02/17   Info  (effectiveness of the Slovak translation)
MSA-I/03 Witness assessment of inspection bodies 02/17 Click for open file    
Certification bodies
Identification Title Effective from PDF Extra Note
MSA-CO/01 Scope and scope specification of accreditation of bodies certifying persons 07/14 Click for open file    
MSA-CO/03 Witness assessment of bodies certifying persons 09/13 Click for open file    
MSA-CP/01 Scope and scope specification of accreditation of bodies certifying products 12/16      
MSA-CP/03 Witness assessment of bodies certifying products 12/16      
MSA-CP/04 EA guidelines on the accreditation of certification of primary sector products by means of sampling of sites (EA – 6/04 M: 2011) 04/13   Info  (effectiveness of the Slovak translation)
MSA-CP/05 Application of ETSI EN 319 403 v2.2.2 (2015-08) for assessment of CAB certifying services according to eIDAS Regulation 05/17      
MSA-CS/01 Scope and scope specification of accreditation of bodies certifying management systems 03/17 Click for open file    
MSA-CS/03 Witness assessment of bodies certifying management systems 12/14 Click for open file    
MSA-CS/04 Certification of organisations with several workplaces based on sampling (IAF MD 1:2007) 08/09   Info  (effectiveness of the Slovak translation)
MSA-CS/05 Transfer of accredited certification of management systems (IAF MD 2:2007) 08/09   Info  (effectiveness of the Slovak translation)
MSA-CS/06 Procedures for advanced surveillance and repeated assessment – ASRP (IAF MD 3:2008) 08/09   Info  (effectiveness of the Slovak translation)
MSA-CS/07 Methods for auditing using computer technology – CAAT (IAF MD 4:2008) 08/09   Info  (effectiveness of the Slovak translation)
MSA-CS/08 Guidelines on the use of EN 45011 AND ISO/IEC 17021 for certification to EN ISO 3834 (EA-6/02) 08/13   Info  
MSA-CS/09 Legal compliance as a part of accredited ISO 14001:2004 certification (EA-7/04) 08/13   Info  
MSA-CS/10 IAF mandatory document for the application of ISO/IEC 17021 for audits of integrated management systems (IAF MD 11: 2013) 03/14   Info  
MSA-CS/11 IAF Mandatory Document for Detarmination of audit time of quality and environmental management systems (IAF MD 5:2015) 06/16   Info  (effectiveness of the Slovak translation)
MSA-CS/12 Food Safety Management Systems – Scope of Accreditation (EA-3/11:2009) 03/10   Info  (effectiveness of the Slovak translation)
MSA-CS/13 Application of ISO/IEC 17021 in the field of medical device quality management systems (ISO 13485) (IAF MD 9: 2015) 10/15   Info  (effectiveness of the Slovak translation)
MSA-CS/14 IAF mandatory document for assessment of certification body management of competence in accordance with ISO/IEC 17021: 2011 (IAF MD 10: 2013) 09/13   Info  
MSA-CS/15 Witnessing Activities For The Accreditation Of Management Systems Certification Bodies In Accordance With IAF MD 17: 2015 03/17 Click for open file    
Environmental Verifiers
Identification Title Effective from PDF Extra Note
MSA-E/01 Scope and scope specification of accreditation of environmental verifiers 04/16 Click for open file    
MSA-E/02 Requirements for environmental verifiers 08/14 Click for open file    
MSA-E/04 Surveillance of environmental verifiers 05/14 Click for open file    
MSA-E/05 Witness assessment of environmental verifiers 07/14 Click for open file    
Notified bodies
Identification Title Effective from PDF Extra Note
MSA-N/01 Accreditation for Notification Purposes (EA-2/17 M: 2016) 02/17   Info  
Good laboratory practice
Identification Title Effective from PDF Extra Note
MSA-G/01 OECD Principles on Good Laboratory Practice (OECD Guideline No. 1) 03/17   Info  
MSA-G/02 Revised Guides for Compliance Monitoring Procedures for Good Laboratory Practice (OECD Guideline No. 2) 03/17   Info  
MSA-G/03 Revised Guidance for the Conduct of Laboratory Inspections and Study Audit (OECD Guideline No. 3) 03/17   Info  
MSA-G/04 Quality Assurance and GLP (OECD Guideline No. 4) 03/17   Info  
MSA-G/05 Compliance of Laboratory Suppliers with GLP Principles (OECD Guideline No. 5) 03/17   Info  
MSA-G/06 The Application of the GLP Principles to Field Studies (OECD Guideline No. 6) 04/17   Info  
MSA-G/07 The Application of the GLP Principles to Short Term Studies (OECD Guideline No. 7) 04/17   Info  
MSA-G/08 The Role and Responsibilties of the Study Director in GLP Studies (OECD Guideline No. 8) 04/17   Info  
MSA-G/09 Guidance for the Preparation of GLP Inspection Reports (OECD Guideline No. 9) 04/17   Info  
MSA-G/11 The Role and Responsibility of the Sponsor in the Application of the Principles of GLP (OECD Guideline No. 11) 03/12   Info  
MSA-G/12 Requesting and Carrying Out Inspections and Study Audits in Another Country (OECD Guideline No. 12) 03/12   Info  
MSA-G/13 The Application of the OECD Principles of GLP to the Organisation and Management of Multi-Site Studies (OECD Guideline No. 13) 03/12   Info  
MSA-G/14 The Application of the Principles of GLP to in vitro Studies (OECD Guideline No. 14) 03/12   Info  
MSA-G/15 Establishment and Control of Archives that Operate in Compliance with the Principles of GLP (OECD Guideline No. 15) 03/12   Info  
MSA-G/16 Guidance on the GLP Requirements for Peer Review of Histopathology (OECD Guideline No. 16) 05/17   Info  
MSA-G/18 OECD Position Paper Regarding the Relationship between the OECD Principles of GLP and ISO/IEC 17025 (OECD Guideline No. 18) 05/17   Info  
Verification
Identification Title Effective from PDF Extra Note
MSA-V/01 Scope and scope specification of accreditation of greenhouse gas verifiers 08/14 Click for open file    
MSA-V/02 IAF mandatory document for the application of ISO 14065: 2013 (IAF MD 6: 2014) 04/14   Info  (effectiveness of the Slovak translation)
MSA-V/03 Witness assessment of greenhouse gas verifiers 04/14 Click for open file    
MSA-V/04 EA Document for Recognition of Verifiers under the EU ETS Directive (EA-6/03 M: 2013) 02/14   Info