- Welcome Guest
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The United Group of Conformity Assessment Bodies (UGCAB), Iraq, is welcomed as a Stakeholder member of ILAC.
We welcome UGCAB and look forward to working with our UGCAB colleagues.
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The Asia Pacific Food Analysis Network (APFAN) and the AOAC South West Pacific (AOAC SWP) Section in association with the University of the South Pacific (USP) Centre for Sustainable Futures and the Chemical Society of the South Pacific (CSSP), welcome you to join the upcoming APFAN PT5 Workshop / AOAC SWP Annual Meeting to be held in Suva in Fiji on 8th – 10th September 2025.
This International Workshop has the theme “Building Sustainable Food Analysis Capacity in the Asia Pacific – Enhancing Global Comparability”.
The Technical Program will cover a number of topics including:
The ISO/IEC 17025:2017 Management System
The ISO/IEC 17025:2017 Technical System
Food Composition and Nutritional Testing
Residue and Toxin Testing in Pacific Products
Analyses for Sustainable Futures
Food Microbiology Testing
Testing of Indigenous / Underutilised Foods
Capacity Building Initiatives in the Asia Pacific
Discussion of PT5 Results
The registration fees and Call for Papers will be made available in early June 2025.
We also acknowledge and welcome participants of the 12th OCEANIAFOODS (INFOODS) meeting on the 12th September – “Indigenous Peoples Food Systems and the Food Composition in Oceania”. Welcome also to members of the Pacific Islands Testing Committee (PITC) under the Pacific Quality Infrastructure Initiative (PQII) and associated national laboratory networks, with meeting rooms available on the 11th and 12th September after this Workshop.
For further information, please contact Stewart Jones, Coordinator, APFAN at: apfan.apfan@yahoo.com
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EIAC launched new accreditation schemes
The Emirates International Accreditation Centre (EIAC) has launched new accreditation schemes for Validation/Verification bodies according to ISO/IEC 17029 and for the Medical Devices Quality Management Systems (MDQMS) certification bodies for ISO 13485 certifications according to ISO/IEC 17021-1 accreditation. Ms. Amina Ahmed Mohammed Chief Executive Officer of EIAC formally launched these schemes in an awareness ceremony in Dubai.
In her address Ms. Mohammed said that the new accreditation scheme for validation/verification bodies is in line with the UAE government’s commitment towards climate change. She noted that greenhouse gases emissions have become a greater challenge over time. And that the accreditation of validation/verification bodies would provide credible platform to the industry to recognise their environmental claims. Ms. Mohammed also said that the growing market of medical devices in UAE would benefit from the new scheme for accreditation of Medical Devices Quality Management Systems certification bodies.
Representatives of conformity assessment bodies and stake holders attended the ceremony.
EIAC CEO Ms. Amina Ahmed formally launching new accreditation schemes.
EIAC hosted APAC ITSMS training in Dubai
EIAC hosted the Asia Pacific Accreditation Cooperation (APAC) training on ISO/IEC 20000-6: Information technology — Service management- Requirements for bodies providing audit and certification of service management systems. Staff and assessors of various accreditation bodies attended the training.
Mr. Abdulla Al Marzooqi director of certification bodies accreditation department of EIAC welcomed all delegates. He also thanked APAC for arranging the training in Dubai. Ms. Seema Khurana of United Accreditation Foundation, USA was the resource person.
EIAC hosted APAC training.
EIAC hosted APAC ISMS, ITSMS and AI Evaluator Workshop in Dubai
EIAC also hosted the APAC workshop for peer evaluators for ISMS, ITSMS and AI, in Dubai. APAC peer evaluators from various accreditation bodies attended the workshop.
EIAC thanked APAC for arranging the workshop in Dubai. Ms. Seema Khurana of United Accreditation Foundation, Mr. Young Jae Park of Korea Accreditation Board (KAB), Mr. Pu-Hsien (Bruce) Li of Taiwan Accreditation Foundation (TAF) and Mr. Zhigao Fu of China National Accreditation Service for Conformity Assessment (CNAS) contributed to the workshop as resource persons.
EIAC hosted APAC peer evaluators’ workshop.
EIAC participated in Arab Health Medical Expo 2025
EIAC participated in Arab Health Medical Expo held on 27 January to 30 January 2025. Arab Health is the largest exhibition and forum of medical field in the region. Many exhibitors of medical products including devices, pharmaceuticals, healthcare service providers and medical professionals attended the exhibition and discussion forums. The EIAC had an information booth in the exhibition. Accreditation information was provided to the visitors. A large number of medical professionals from the healthcare sector, including medical laboratories, visited the EIAC booth.
EIAC’s participation in Arab Health.
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In these days, teamwork, transparency and collaboration are essential for innovation. Reality is changing and there is an increasing use of digital means and formulation of work processes through them. Accreditation must be present in these processes and ensure that those engaged in the profession are aware of and act within the framework of the accreditation principles.
The direct impact is already evident today. Basic processes are answered by the various AI softwares. Some of the answers they receive are AI-based and we must check and ensure that there is indeed an appropriate response to the findings when performing activities to test professional competence. The use of technological means must be in accordance with national, regional and international requirements. Those who participate influence these activities.
We are involved on a regular basis in the activity and, as required, in supporting our partners in our activities and those who have signed MOU’s with us.
The parallel work required these days at ILAC and Global Accreditation Cooperation Incorporated requires many hours of meetings reviewing documents and agreements between all members. Thanks to all those involved in the work, the consultants to the Secretariat and the representatives who volunteer their time and expertise. They work for the success of our activities and the implementation of the decisions of all ILAC members.
Read MoreILAC Meetings
The IAF/ILAC Mid-term meetings were held virtually during March/April 2025.
The next IAF/ILAC annual meetings will be held as an in-person event in Bangkok, Thailand from 15 – 24 October, 2025.
In addition to the in-person meetings noted above all ILAC Committees, Working Groups and Task Forces continue to progress the items on their work plans, via a combination of email and remote meetings.
Information on future meetings and events, including major regional meetings, can also be found in the ILAC Calendar.
Decision to Establish a Single International Organisation for Accreditation
Following extensive work and discussions within IAF and ILAC in 2024 the IAF and ILAC membership agreed the Constitution and General Rules for a new organisation, to take over the existing roles of both IAF and ILAC. Following the annual meetings of IAF and ILAC in October 2024, the Global Accreditation Cooperation Incorporated was registered in New Zealand.
The launch date for the Cooperation to become operational and to take over the roles of IAF and ILAC, is provisionally 1 January 2026. Further information on the transition and exact date will be publicised shortly.
The ILAC MRA
The scope of recognition of the recognised regions to the ILAC MRA is available from Recognised Regional Cooperation Bodies International Laboratory Accreditation Cooperation (ilac.org)
Information on the acceptance of calibration, testing and inspection results programs provided by PTPs and reference materials produced by RMPs via the ILAC MRA is available from ILAC MRA and Signatories International Laboratory Accreditation Cooperation.
There are currently 118 signatories to the ILAC MRA representing 119 economies. The ILAC MRA covers recognition for accreditation in the areas of calibration (ISO/IEC 17025), testing (ISO/IEC 17025), medical testing (ISO 15189), inspection (ISO/IEC 17020), proficiency testing providers (ISO/IEC 17043) and reference material producers (ISO 17034). The list of signatories to the ILAC MRA is available from the ILAC MRA Signatory Search.
The ILAC MRA Annual Report 2024 and associated Infographic will be published shortly, and members will be notified by email. The documents will be uploaded to the ILAC Website when available.
Case studies and research on the recognition of the ILAC MRA by governments and regulators are available from the Public Sector Assurance website. The website is a collaborative initiative of the INetQI members and there are over 330 case studies, 90 research papers and 60 supporting materials available to view.
The Business Benefits website is a reference website designed to demonstrate the monetary value of standards, conformity assessment and accreditation for businesses. The website represents another successful collaboration of the INetQI partners with over 95 case studies categorised into 6 areas of value. All of the case studies identify a clear financial benefit. The site also includes more than 75 research papers.
Both the Public Sector Assurance and the Business Benefits websites contain a dedicated search function for each of the 17 United Nations Sustainable Development Goals (SDGs). The case studies on these sites are now all linked to applicable goals.
ILAC Membership
The ILAC membership as of 31 March 2025 is:
The ILAC membership consists of 161 organisations from 135 different economies worldwide. Over 114,600 laboratories, over 15,600 inspection bodies, over 700 PTP and over 300 RMP are accredited by the ILAC Full Members (signatories to the ILAC MRA).The latest statistics and graphs on the number of accreditation bodies, accredited laboratories, inspection bodies, PTPs and RMPs are available from the ILAC Facts & Figures page.
ILAC Executive Committee
In 2024 the Executive Committee met virtually and held in-person meetings. The first meeting for 2025 was held on 30 April.
The IAF and ILAC Joint Executive Committee (JEC) held four (4) meetings in 2024 (February, June, September and October). The first meeting for 2025 was held on 3 April.
ILAC Liaisons and other International Activities
The current list of ILAC liaison activities includes:
ILAC Liaisons with ISO and ISO/CASCO Policy Committees
ILAC Liaisons with ISO/CASCO Working Groups/Task Forces
ILAC Liaisons with Other Organizations
ILAC thanks all the ILAC liaison officers, and their organisations, who volunteer their time to assist ILAC in carrying out these activities for the benefit of all ILAC members.
Information on ILAC’s partnerships, including copies of communiqués, joint procedures, press releases and MoUs is available from the ILAC Partnerships Page.
ILAC Secretariat
There have been no changes to Secretariat staff since the last newsletter.
Documents and Brochures
Publications finalised and released in 2024 include:
ILAC-P9:01/2024 ILAC Policy for Proficiency Testing and/or Interlaboratory comparisons other than Proficiency Testing
Follow @ILAC_Official on “X” or ILAC on LinkedIn to receive the latest ILAC news, including information on meetings, events, liaison activities and new publications.
The November 2024 edition of the ILAC Newsletter is available from News-and-Events/ILAC Newsletter/Archive (ilac.org). The next edition will be published in November 2025.
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The Spring Laboratory Committee Meeting
The Laboratory Committee met on 26 and 27 March in Bratislava, Slovakia, to discuss the following topics:
Following the summary report on the WS Subcontracting, a breakout session will be held during the next LC meeting in September 2025 to focus on policy related to:
The EA LC Working Group (WG) Health Care
The EA LC Working Group (WG) Health Care met in Skopje, North Macedonia, on 5 and 6 December.
Members attended a half-day workshop regarding challenges encountered in the transition of accreditation of medical laboratories to EN ISO 15189:2022. The outcome of the 7 working groups will be used for the coming meetings of the WG.
During the meeting, several items were presented and discussed:
In addition, participants discussed several questions, such as concerning, metrological traceability, validation and verification issues, and reporting of results. New periodic work items that may be discussed in the WG are related to Artificial Intelligence (AI) used in medical analysis.
The longtime convener of the WG, Rolf Straub, SAS (the Swiss NAB), convened his last meeting and handed over the lead to Hélène Méhay, COFRAC (the French NAB), who started her term in January 2025.
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In the Republic of Uzbekistan, a robust mechanism is in place to monitor the health status of the population, ensure the provision of quality medical care, and enforce international standards in the production of medical equipment. This sector is governed by a series of resolutions and pertinent documents issued at both governmental and ministerial levels.
The Government has actively adopted international standards to safeguard public health, including those defined by the International Organization for Standardization (ISO). Notably, standards such as ISO 15189 and ISO 13485 have been introduced in recent years to enhance the quality of medical services and products.
The quality infrastructure in Uzbekistan is increasingly focused on integrating these standards and evaluating compliance during accreditation processes. The National Accreditation System prioritises the expansion of the service sector, recognising its vital role in ongoing development and public welfare. While the achievement of international recognition is commendable, the ongoing maintenance and improvement of standards remain critical.
The State Enterprise Uzbek Center for Accreditation (O’ZAKK) successfully achieved international recognition in several scope, including in Medical Device Quality Management Systems as per ISO 13485. This standard emphasises quality management systems in the production of medical devices and has received official recognition under the International Accreditation Forum (IAF) Multilateral Recognition Arrangement (IAF MLA).
In Uzbekistan, both state-owned and private enterprises, ranging from large corporations to small businesses, are engaged in manufacturing of medical equipment. The quality of these medical products has a direct bearing on public health, making the production of safe medical devices a fundamental governmental responsibility in safeguarding consumer rights.
A comprehensive set of legal instruments governing product safety has been developed and implemented in Uzbekistan. Currently, the state register indicates that over 100 types of medical products are manufactured within the country.
Prior to the establishment of the national accreditation body for certifying management system certification bodies for medical device manufacturers, products had already been evaluated by certification bodies against established standards. The training of experienced assessors and the creation of a qualified service that complies with ISO 13485 are essential tasks within the National Accreditation System today.
Moreover, the push for competitiveness and quality within the industry has led to an expansion of accreditation services. In this regard, O’ZAKK has collaborated with leading accreditation bodies in the Asia-Pacific region, including the Korea Accreditation Board (KAB), achieving favorable outcomes. The qualifications of Uzbek assessors have been significantly enhanced through participation in various international training programs.
As part of a pilot project, one certification body has successfully obtained accreditation and is currently conducting audits to issue certificates of conformity to medical device manufacturers. Additionally, two more certification bodies are undergoing the accreditation process for this standard.
This progress signifies an improvement in the qualifications of Uzbek assessors and the introduction of new directions within the field. It not only fosters increased competition in the domestic market but also expands the options available to manufacturers.
Furthermore, the certification of accredited management systems serves as an effective mechanism for protecting the interests of consumers, regulators, and the broader public, particularly in the healthcare sector.
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AFRAC HOLDS TRAINING WORKSHOP ON DECISION MAKING INCLUDING THE ROLE OF THE TASK FORCE GROUP
The African Cooperation in Accreditation (AFRAC) recently organised and conducted a virtual training workshop Decision Making Including the Role of Task Force Groups (TFG). The workshop, sponsored by PTB Germany, was held over two half-days on 14 and 15 January 2025. It was attended by a total of thirty (30) participants drawn from AFRAC and Southern African Development Community cooperation in Accreditation (SADCA) MRA Committee and Council members, peer evaluators, trainee peer evaluators and TFG members.
AFRAC is a cooperation of accreditation bodies (national and multi-economy), National Accreditation Focal Points (NAFP), sub-regional accreditation cooperations and stakeholders. The objective of AFRAC is to provide internationally recognised and accepted accreditation support to industry and to contribute to the protection of health and safety of the public and the protection of the environment, thereby facilitating trade and contributing to the improvement of Africa’s competitiveness within the global market. The AFRAC MRA Committee plan and manage the implementation and maintenance of AFRAC’s MRA. Peer evaluations are undertaken by a pool of qualified and registered peer evaluators. Decisions on and management of membership in the MRA is the responsibility of the MRA Council. The AFRAC MRA Committee and Council membership has been changing over the years with new members being admitted. Peer evaluators are also continually being trained, qualified, upgraded and registered.
The last training on AFRAC Decision Making Process was held on 6 July 2023. However, some new members of the MRA Committee/Council peer evaluators and trainee peer evaluators have not yet been trained. AFRAC-related documents are continuously being revised/developed. All those involved are required to be fully aware of the decision-making process and follow it consistently at all times. It is for this reason that AFRAC arranged the January workshop.
The Training workshop which was facilitated by Mrs. Maureen P Mutasa was opened by the AFRAC Secretariat, Ms. Fikile Skosana who welcomed the participants, wished them a successful workshop and declared the training workshop open. The Facilitator, welcomed participants from both AFRAC and SADCA, introduced herself and gave background to the training workshop. She then asked participants to introduce themselves outlining their name, position in AFRAC/SADCA, name of accreditation body and position in accreditation body (AB). She informed participants about the objective of the training workshop, which was to impart knowledge on decision-making processes regarding evaluations of an AB including the role of the TFG, and to exchange experiences and knowledge through group discussions, so as to ensure consistent and harmonised decision making.
In her opening remarks the Facilitator thanked PTB Germany for sponsoring the training, the AFRAC Secretariat for her engagement and more importantly the opportunity to share knowledge and experiences, noting that the Facilitator was the immediate past AFRAC MRA Council chair, MRA Committee member and also served on the International Accreditation Forum (IAF) decision making body on evaluations IAF Multilateral Arrangement Committee (MLAC) amongst many other positions in AFRAC, SADCA, IAF and ILAC.
The Facilitator started the workshop by giving an overview of the AFRAC peer evaluation process, highlighting the relevant evaluation documents, some of which had been revised since the last training, the purpose of evaluations, the stages in the evaluation process, establishment of a TFG, consideration of the final evaluation report, and TFG summary review before submission to the MRA Council for decision making.
After the break, the Facilitator presented the terms of reference of the MRA Council covering the functions, composition, responsibilities, meetings and voting rights of MRA Council members. She then outlined the decision-making process, highlighting the role of all the players in this process. Time was spent on the competences and role of the TFG. The Facilitator then walked participants through F017: TFG Evaluation Summary Report and Recommendations to the MRA Council. She outlined all the 10 sections of F 017 and what information was to be completed under each section.
On Day 2 the Facilitator started by presenting two examples of duly completed F 017, highlighting the comments made, collaborations of the TFG with the Evaluation Team and the AB, and the recommendations. She recapped on the subjects covered on Day 1 of the workshop. She also explained classification and closing of findings from evaluations, which members should have a good understanding of, as this is an aspect for consideration in reviewing final evaluation report. She outlined the decision-making process and how, through the process as outlined in AFRAC M001, the MRA Council ensures fair, professional and impartial decisions. The documents for review by the MRA Council in the decision-making process were laid out as were the stages leading to the decisions. The timelines for the processes were highlighted, to ensure timely decisions. The Facilitator also covered the hierarchy of decisions on new applicant AB and MRA signatories, including reasons for and consequences of suspensions/withdrawal. Decisions on joint evaluations were also covered in detail.
Throughout the workshop the participants asked many questions and made numerous comments which were discussed by the group, drawing on the experiences of some of the participants. Areas of improvement to the MRA processes were identified. The interactions throughout the training workshop were very.
Based on feedback from the participants the overall feedback was that the workshop was well planned, organised and presented, and the content was very relevant. Training materials were circulated by the AFRAC Secretariat to all participants and those who were unable to attend the
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EUROLAB is delighted to partner with different organisations to host various upcoming events, which will allow laboratory and conformity assessment professionals, researchers, as well as other interested stakeholders, to gain valuable insights into best practices, validation processes, and key challenges in measurement procedures and certified reference materials. Participants will have the opportunity to engage with experts, explore real-world applications, and enhance their understanding of critical industry standards and trends.
EUROLAB and Eurachem will co-host a webinar “How to Validate Measurement Procedures Including Sampling (VaMPIS).” The event will take place on 19 June from 10:00 – 13:00 CET, online via Zoom.
High-level speakers and authors of the VaMPIS guide will provide valuable insights on the key best practices and validation of measuring procedures, with practical examples and guidelines. Moreover, guidance on the applications of VaMPIS to in-situ and ex-situ measurements will be provided. The management of the whole measurement process, including follow-up after validation will also be a topic of discussion during the webinar.
Participants will have the opportunity to address questions and further clarify any possible uncertainties directly with the authors and experts in the field during the roundtable discussion.
The event is free-of-charge and you can register at the following registration link.
EUROLAB-ASSOTIC Seminar
On Wednesday, September 17 from 10:00-13:00 CEST, EUROLAB and ASSOTIC will host a seminar on Certified Reference Materials – trends, challenges & opportunities alongside the IMEKO Joint Conference TC8-TC11-TC24, in Torino, Italy.
Certified Reference Materials (CRMs) play a critical role in analysing and testing, by providing standardised and traceable benchmarks to ensure the reliability, accuracy, and consistency of measurements and analytical results. Laboratories can ensure the reliability of their data, build trust with clients, and comply with industry and regulatory standards by using CRMs. However, there are several challenges when it comes to the use of CRMs. The seminar aims to offer an overview of the current context, trends and critical issues, with the intent of enhancing dialogue among the different affected groups, while sharing best practices.
If you are interested in attending the seminar, you can register here: Registration page.
See our website for all recent news and updates
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1. 12th ARAC Annual Meetings: Advancing Accreditation and Strategic Vision
The 12th Annual Meetings and General Assembly of the Arab Accreditation Cooperation (ARAC) were successfully held on December 18-19, 2024, in Makkah, Saudi Arabia, hosted by the Saudi Accreditation Center (SAAC).
The event brought together over 50 participants from Arab Accreditation Bodies and key stakeholders, marking a pivotal moment for regional collaboration in accreditation. Key achievements included the enhancement of ARAC MLA signatories’ recognition scopes, the extension of the ARAC MLA structure, and the acceptance of new stakeholders. A major highlight was the launch of the development process for the new ARAC Strategy 2026-2030, which aims to align accreditation practices with emerging global trends and sustainable development goals.
These milestones reinforce ARAC’s role as a leading accreditation body, fostering confidence in regional and global trade while supporting sustainable economic growth across the Arab region.
2. New ARAC Stakeholder member: United Group of Conformity Assessment Bodies (UGCAB)
Significant growth ARAC membership has been achieved with the acceptance of the Saudi Green Building Forum (SGBF), KSA, as an ARAC Stakeholder Member in March 2025.
The participation of interested parties in ARAC fulfills two primary objectives. First, it strengthens trust among stakeholders in the accreditation process. By engaging a broad spectrum of voices—including industry representatives, regulatory authorities, conformity assessment bodies (CABs), and consumers—ARAC reinforces the transparency, credibility, and acceptance of its accreditation framework. This inclusive approach facilitates mutual recognition of ARAC’s systems, a critical factor in advancing quality infrastructure throughout the Arab region.
Second, stakeholder involvement enables these parties to actively share insights and feedback with ARAC. Their contributions help shape policies, technical standards, and conformity assessment practices, ensuring alignment with sector-specific needs and expectations. This collaborative dialogue keeps ARAC adaptive to market trends, regulatory changes, and technological developments. Moreover, it fosters the harmonisation of accreditation practices, reducing trade barriers and promoting compliance with international standards across member states.
3. ARAC Capacity Building activities
As part of the ARAC Capacity Building Committee’s program implementation, and in line with efforts to strengthen the skills of personnel from ARAC Accreditation Bodies (ABs) and ARAC Peer Evaluators involved in the accreditation process, the following capacity-building initiatives have been successfully conducted:
3.1. Workshop on the New ILAC P9:1/2024 Policy – 19th & 20th November 2024
This workshop focused on the implementation of the new version of ILAC P9, with the main objectives as the following:
3.2. ARAC Regional Transition Workshop for ISO 15189:2022 – 25th & 26th December 2024
This workshop covered the following topics
3.3. ARAC Regional Training Workshop on ISO/IEC 17029 and ISO 14065 – 13th & 14th January 2025
This workshop organised as part of the ARAC Capacity Building Committee’s Work Plan, aimed to achieve the following main objectives:
4. Activities to Promote the IAF MLA and ILAC MRA:
A study has been developed to assess the impact and benefits of accreditation in the Arab Region, employing a two-pronged approach. The study aims to:
a. Comprehensively evaluate the advantages of accreditation across the Arab region, with a focus on its impact on key areas such as:
b. Assess the impact of strengthening the accreditation ecosystem, including:
5. ARAC Unveils Comprehensive Approach for Developing New Strategy 2026-2030:
The ARAC strategic development process for the ARAC Strategy 2026-2030 has been launched, marking a significant step toward strengthening the region’s accreditation infrastructure. A dedicated Steering Committee has been established to oversee and guide the strategy’s development, ensuring it aligns with ARAC’s long-term vision and the evolving needs of its members and stakeholders.
The new strategic framework will prioritise enhancing ARAC’s role in promoting quality, fostering collaboration, and supporting the sustainable growth of the Arab accreditation system. To achieve this, the development process will include extensive consultations with members and stakeholders, ensuring the strategy is both forward-thinking and responsive to the dynamic challenges and opportunities within the accreditation landscape.
This comprehensive approach underscores ARAC’s commitment to advancing regional cooperation, driving innovation, and maintaining high standards of accreditation across the Arab world. The ARAC Strategy 2026-2030 is set to play a pivotal role in shaping the future of accreditation, ensuring it remains robust, inclusive, and adaptable to the changing global environment.
6. 6th Edition of the Arab Accreditation Week:
The 6th Edition of the Arab Accreditation Week 2025, AA 2025, will be held in June 2025 under the theme “How Accreditation Empowers Small and Medium Enterprises (SMEs) in the Arab Region,” the event will highlight the critical role of accreditation in enhancing SME competitiveness, market access, and trust.
The week-long program will feature capacity-building workshops, awareness sessions, and panel discussions with key stakeholders, including policymakers, industry leaders, conformity assessment bodies, and SME representatives. Participants will explore how accredited conformity assessment supports SMEs in meeting regulatory requirements, improving product quality, and expanding into regional and global markets.
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