12/30254927 DC : 0
Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
BS EN 16372 - AESTHETIC SURGERY SERVICES
Available format(s)
Hardcopy , PDF
Superseded date
01-31-2015
Language(s)
English
Publisher
Foreword
Introduction
1 Scope
2 Terms and definitions
3 Competencies
4 Management and communication with patients
5 Facilities
6 Procedures
7 Quality assurance and improvement
Annex A (normative) - Code of Ethics for marketing
and advertising
Annex B (informative) - UEMS
Bibliography
BS EN 16372
| Committee |
CH/403
|
| DocumentType |
Draft
|
| Pages |
38
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| SupersededBy |
| Standards | Relationship |
| PREN 16372 : DRAFT 2013 | Identical |
| ISO 10001:2007 | Quality management Customer satisfaction Guidelines for codes of conduct for organizations |
| ISO 18308:2011 | Health informatics — Requirements for an electronic health record architecture |
| EN ISO 80601-2-61:2011 | Medical electrical equipment - Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment (ISO 80601-2-61:2011) |
| ISO 19011:2011 | Guidelines for auditing management systems |
| ISO 80601-2-13:2011 | Medical electrical equipment Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation |
| ISO 16054:2000 | Implants for surgery Minimum data sets for surgical implants |
| EN ISO 10781:2015 | Health Informatics - HL7 Electronic Health Records-System Functional Model, Release 2 (EHR FM) (ISO 10781:2015) |
| EN ISO 15225:2016 | Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2016) |
| ISO 31000:2009 | Risk management Principles and guidelines |
| ISO 26000:2010 | Guidance on social responsibility |
| ISO 13485:2016 | Medical devices Quality management systems Requirements for regulatory purposes |
| EN ISO 27789:2013 | Health informatics - Audit trails for electronic health records (ISO 27789:2013) |
| ISO/TS 21547:2010 | Health informatics Security requirements for archiving of electronic health records Principles |
| EN ISO 21090:2011 | Health Informatics - Harmonized data types for information interchange (ISO 21090:2011) |
| ISO 25424:2009 | Sterilization of medical devices Low temperature steam and formaldehyde Requirements for development, validation and routine control of a sterilization process for medical devices |
| ISO/IEC 27002:2013 | Information technology Security techniques Code of practice for information security controls |
| ISO 11810-2:2007 | Lasers and laser-related equipment Test method and classification for the laser-resistance of surgical drapes and/or patient-protective covers Part 2: Secondary ignition |
| ISO 21090:2011 | Health informatics — Harmonized data types for information interchange |
| ISO 10003:2007 | Quality management Customer satisfaction Guidelines for dispute resolution external to organizations |
| ISO 11135-1:2007 | Sterilization of health care products Ethylene oxide Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices |
| ISO 14630:2012 | Non-active surgical implants General requirements |
| EN ISO 16054:2002 | Implants for surgery - Minimum data sets for surgical implants (ISO 16054:2000) |
| EN ISO 25424:2011 | Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2009) |
| IEC TR 60825-8:2006 | Safety of laser products - Part 8: Guidelines for the safe use of laser beams on humans |
| ISO 18812:2003 | Health informatics — Clinical analyser interfaces to laboratory information systems — Use profiles |
| ISO 16061:2015 | Instrumentation for use in association with non-active surgical implants General requirements |
| ISO 10002:2014 | Quality management Customer satisfaction Guidelines for complaints handling in organizations |
| 2006/25/EC : 2006 AMD 3 2013 | DIRECTIVE 2006/25/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL OF 5 APRIL 2006 ON THE MINIMUM HEALTH AND SAFETY REQUIREMENTS REGARDING THE EXPOSURE OF WORKERS TO RISKS ARISING FROM PHYSICAL AGENTS (ARTIFICIAL OPTICAL RADIATION) (19TH INDIVIDUAL DIRECTIVE WITHIN THE MEANING OF ARTICLE 16(1) OF DIRECTIVE 89/391/EEC) |
| ISO 11810-1:2005 | Lasers and laser-related equipment Test method and classification for the laser resistance of surgical drapes and/or patient protective covers Part 1: Primary ignition and penetration |
| EN ISO 11135-1:2007 | Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007) |
| ISO 14644-1:2015 | Cleanrooms and associated controlled environments Part 1: Classification of air cleanliness by particle concentration |
| ISO 80601-2-61:2011 | Medical electrical equipment Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment |
| EN ISO 14971:2012 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) |
| EN ISO 16061:2015 | Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2015) |
| ISO 15225:2016 | Medical devices Quality management Medical device nomenclature data structure |
| ISO/HL7 10781:2015 | Health Informatics — HL7 Electronic Health Records-System Functional Model, Release 2 (EHR FM) |
| EN ISO 18812:2003 | Health informatics - Clinical analyser interfaces to laboratry information systems - Use profiles (ISO 18812:2003) |
| EN ISO 11810-1:2009 | Lasers and laser-related equipment - Test method and classification for the laser resistance of surgical drapes and/or patient protective covers - Part 1: Primary ignition and penetration (ISO 11810-1:2005) |
| ISO/TR 21548:2010 | Health informatics Security requirements for archiving of electronic health records Guidelines |
| EN ISO 17665-1 : 2006 | Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006) |
| ISO 14971:2007 | Medical devices Application of risk management to medical devices |
| EN ISO 27799:2016 | Health informatics - Information security management in health using ISO/IEC 27002 (ISO 27799:2016) |
| ISO 14607:2007 | Non-active surgical implants Mammary implants Particular requirements |
| EN ISO 14644-1:2015 | Cleanrooms and associated controlled environments - Part 1: Classification of air cleanliness by particle concentration (ISO 14644-1:2015) |
| EN ISO 11810-2:2009 | Lasers and laser-related equipment - Test method and classification for the laser-resistance of surgical drapes and/or patient-protective covers - Part 2: Secondary ignition (ISO 11810-2:2007) |
| ISO 17665-1:2006 | Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices |
| EN ISO 14630:2012 | Non-active surgical implants - General requirements (ISO 14630:2012) |
| ISO 27799:2016 | Health informatics Information security management in health using ISO/IEC 27002 |
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