IMDRF Project: List of international standards recognized by IMDRF management committee members

Similar documents
IVD Regulatory Update February 2015

Post Market Surveillance (PMS): National Competent Authority Report (NCAR) Exchange Programme under IMDRF

FINAL DOCUMENT. Global Harmonization Task Force

CMDCAS Handbook Policies and Procedures for Sector Qualification under the Canadian Medical Devices Conformity Assessment System (CMDCAS)

Introduction of AHWP. IMDRF Stakeholder Meeting 25 March 2015

Observers Takuya Noro MHLW X X X Hideto Yokoi PMDA Advisor X X X Adriana Gamboa INFARMED X X X

Introduction of Saudi Arabia Medical Device Regulatory System Ali Al Dalaan Executive Director, SFDA AHWP TC Chair

International Medical Device Regulatory Harmonization. Reality or Fantasy?

Accreditation of Clinical Laboratories

Software Regulation and Validation

IAF Mandatory Document for the Application of ISO/IEC in Medical Device Quality Management Systems (ISO 13485)

SUMMARY REPORT OF THE 17 th ACCSQ MDPWG MEETING

Recent Development of ICH GCG

International trend on medical device regulatory convergence

EPEAT Requirements of PREs

FINAL STATUS DOCUMENT

ICH Regulators Forum. Dr Peter Arlett EU

IECEx OPERATIONAL DOCUMENT

PATHWAYS FOR STANDARDS DEVELOPMENT. Developing internationally aligned Australian Standards in the national interest

Specific Accreditation Criteria Human Pathology. NATA/RCPA accreditation surveillance model for Human Pathology

Content Sheet 11-1: Overview of Norms and Accreditation

International Classification for Nursing Practice (ICNP ) Programme

Consulting Opportunity to Support In-Country Capacity Building Workshops on Declaration of Origin under AANZFTA [AANZ-0077-ROO-12]

Standards for improvement in health care: supervision, certification and accreditation in Europe

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE

GCP Inspection by PMDA

MAY 22-24, 2017 BERLIN (GERMANY)

Guide to Assessment and Rating for Services

IVDD revision changes to the European regulation of in-vitro diagnostic (IVD) Medical Devices. Med-Info. TÜV SÜD Product Service GmbH

Regulatory Control of Diagnostics in Tanzania. Hiiti Sillo Ag. Director General Tanzania Food and Drugs Authority

NZS/ISO 15189:2007. Medical Laboratories Particular Requirements for Quality and Competence NZS/ISO 15189:2007

BRIDGING GRANT PROGRAM GUIDELINES 2018

Consideration on Global Harmonization

Application form for Associated Membership

April 17, Edition of the Joint Commission International Accreditation. SUBJECT: MITA Feedback on the 5 th Standards for Hospitals

EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE

ANVISA - Enhancing marketing authorization of drugs and medical devices in accordance to the international best practices

Regional Alignment in Asia Pacific -

Which QMS Standard should be chosen for the structural quality of a medical laboratory? Matthias ORTH

IOAS Inc. IOAS Operating Manual. information and requirements specific to surveillance under the. Canada Organic Regime

Workshop of APEC Nearly /Net Zero Energy Building Roadmap responding to COP21

Innovation for Safety: achievements and challenges A notified body perspective

Feedback on SADC Workshop of Industry & Regulators. Luther Gwaza PhD Consultant

National Disability Insurance Scheme (Approved Quality Auditors Scheme) Guidelines 2018

CANCER COUNCIL SA BEAT CANCER PROJECT PRINCIPAL CANCER RESEARCH FELLOWSHIP PACKAGES FUNDING GUIDELINES

Productivity, Globalisation, and Sustainable Growth

CANCER COUNCIL SA BEAT CANCER PROJECT TRANSLATIONAL RESEARCH PACKAGES FUNDING GUIDELINES

GLOBAL BIOANALYSIS CONSORTIUM on harmonization of bioanalytical guidance 2014, time for a status update

Quality Risk Management ICH Q9

GLOBAL MARKET ACCELERATION FUND (GMAF) Program Guidelines

Secretary-General of the European Commission, signed by Mr Jordi AYET PUIGARNAU, Director

Summary 12 th GHTF Steering Committee Meeting

Trends in the development of regulatory systems by the example of ICH countries

Performance audit report. Effectiveness of arrangements to check the standard of rest home services: Follow-up report

GHTF SG 3 Final- Meeting Minutes June 7 to 11, 2010 Los Angeles, California, USA

Carbon Sequestration Leadership Forum

Excerpts from the IFHRO Handbook on Health Record Education

NBOG Report for the period

ASSE International Seal Control Board Procedures

Therefore the provision of medicines is an area for which a Community regulatory framework should be properly supervised to ensure full and

ICH STEERING COMMITTEE October 24-29, 2009 St. Louis, MO, USA SUMMARY

The Mineral Products Association

International Sourcing measurement issues. Peter Bøegh Nielsen Statistics Denmark

Suggestions for Modification of the Clinical Trials Directive ELN Annual Meeting 01 February 2011

Designation of Australian conformity assessment bodies for medical devices Implementation, Version 1.0, November 2016

Papua New Guinea Church Partnership Program Phase 2 EVALUATION - UnitingWorld (Australia) and the United Church in PNG.

Report on APEC-Funded Medical Device Delegation Visit Program to Australia, and Canada and the United States

Abu Dhabi Occupational Safety and Health System Framework (OSHAD-SF) Mechanisms

International Cooperation through Horizon IGLO Brussels, 25 February 2016

Reflection Paper on Medicinal Product Supply Shortages Caused by Manufacturing/GMP Compliance Problems. Outcome of 10 September 2012 Workshop

Slovenian legal metrology in the field of health

National Accreditation Board for Certification Bodies. Accreditation Procedure. for. Energy Management Systems Certification Bodies

The Basic Principles of Developing Standards for Accreditation. Triona Fortune Deputy Chief Executive Officer 25 November 2014

THE NATIONAL INVESTMENT IN RESEARCH. Professor Vicki Sara Chair, Australian Research Council

PRACTICAL APPLICATION OF ISO BY ACCREDITATION BODIES - A comparison with ISO/IEC Page 128. ejifcc2004vol15no4pp

Cartel Working Group Work Plan

METS Ignited Mining Equipment Technology Services

A framework guide for Schools and Community Buildings (SCB2)

Safer Sharps? A barometer of take-up in the UK

Committee on the U.S. Commitment to Global Health

IAF MLA Document. Policies and Procedures for a MLA on the Level of Single Accreditation Bodies and on the Level of Regional Accreditation Groups

Pre-Departure Guide Published October 2014 CRICOS Provider No F

Overview of the National Institute for Occupational Safety and Health Respirator Approval Program and Post Market Activities

STANDARD OPERATING PROCEDURE

Hospital and Other Healthcare Facilities

GUIDE TO ENTRY. For further information contact the awards team at

BACKGROUND PAPER THE WEST AFRICA QUALITY SYSTEM PROGRAMME (PHASE 3)

Accreditation Guidelines

Promoting Hong Kong as the Bridgehead for Mainland Enterprises Outward Investment Ventures

Health Research Cluster Tactical Research Project Applications Guidelines for Applicants

Procedure for handling applications for authorisation and review reports under REACH

Assessment of emergency medical services preparedness in the framework of national crisis management structures in EU member states

Working document QAS/ RESTRICTED September 2006

ERN Assessment Manual for Applicants 2. Technical Toolbox for Applicants

ectd IV: It s Almost As Fun As Super Bowl XLIX DIA eregulatory and Intelligence Annual Conference Disclaimer

Sponsorship guidance for all accredited activities

Proposal Form for Standards Development Projects. Version: 2.0 Issued: March 2010

Guidance for Authorities. Submitting a Proposal to host the. International Conference of Data Protection and Privacy Commissioners

Update on Turkey s PMR Project

Transcription:

List of international standards recognized by IMDRF management committee members Progress Report Dr. Matthias Neumann Federal Ministry of Health Germany matthias.neumann@bmg.bund.de Sydney, 25.9.2012

Mandate: 2 Steps IMDRF Project: List of recognised standards 1. Gathering information and creating a list of standards used for medical devices regulatory purposes that are recognized by IMDRF Management Committee members 2. Development of a procedure to continuously enhance the established list

Background: The GHTF regulatory model is based on the principle that the regulation defines the essential principles for safe and effective medical devices. International Standards should specify (interpret) in detail how medical devices (processes or manufacturers) could come into regulatory compliance (e.g. with the essential principles).

Background: The GHTF paper Role of Standards in the Assessment of Medical Devices GHTF/SG1/N044:2008 states: International standards, such as basic standards, group standards and product standards, are a tool for harmonizing regulatory processes to assure the safety, quality and performance of medical devices.... Regulatory Authorities should encourage the use of international standards. Regulatory Authorities should establish a mechanism for recognizing international standards to provide manufacturers with a method of demonstrating conformity with the Essential Principles. This mechanism should also include a procedure for withdrawal of recognition....... Every Region should have established (or should be in the process of establishing) or is using a list of recognized standards.

Initiated Actions: 1. Request for the nomination of national experts 2. Circulation of a first (incomplete) list of more then 720 valid international standards on Medical Devices (ISO/IEC) to USA, Canada, Australia, Japan, Brasil and the EU-Commission 3. Indication of the level of recognition of these standards (Y- fully recognized, N-not recognized, P-partially recognized) by the nominated national experts 4. First Compilation and Assessment of the provided answers

First results: all concerned 6 IMDRF members provided input to the project a list with a clear indication of fully or partially recognized standards was provided by 5 of the 6 regions/countries The number of fully recognized standards (out of 727 standards) varies between 222 and 18 The number of fully and/or partially recognized standards varies between 240 and 45 Out of the provided 727 standards there is no standard which is fully recognized by all participating regions/countries There are 17 standards which are fully recognized by 4 out of 5 regions/countries

Next Steps: Completion of the survey (an additional list of around 430 standards is ready for distribution) Verification and validation of the provided information/indications Clarification and/or establishment of a common interpretation of the term recognized standard (including fully and partially recognized) Finalisation of the information gathering phase Timeline: Spring 2013? Publication of the list of recognized standards IMDRF Management Committee assessment/decision: to establish (probably in cooperation with international standard organisations) a procedure to update, enhance the list of recognized standards

ISO 5840 ISO 10993-3 ISO 10993-4 ISO 10993-6 ISO 10993-7 ISO 10993-14 ISO 10993-15 ISO 10993-17 List of Standards which are fully recognized by 4 out of 5 regions/countries ISO 11135-1 ISO 11137-1 ISO 11607-1 ISO 11607-2 ISO 11737-1 ISO 14155 ISO 14937 ISO 17664 ISO 17665-1

List of international standards recognized by IMDRF management committee members Progress Report Dr. Matthias Neumann Federal Ministry of Health Germany matthias.neumann@bmg.bund.de Sydney, 25.9.2012