Submitted by admin on Wed, 09/28/2016 - 22:13

Global Harmonization Working Party Strategic Framework Towards 2020
“The Foreseeable Harmonization Horizon”
(Version SPR 04a)


The Global Harmonization Working Party (GHWP) was established in 1999 as a voluntary group of regulators and industry members whose goal is to promote regulatory harmonization on medical device regulations in Asia and other regions in accordance with GHTF guidance. With the joint efforts of regulators and industry members over the past 12 years, GHWP has built important momentum:

- Membership: The membership of GHWP has been expanded to 23 economies, covering the Asia Pacific, Latin America and Middle East regions. The current members of GHWP includes: Abu Dhabi, Brunei Darussalam, Cambodia, Chile, China, Chinese Taipei, Hong Kong SAR, India, Indonesia, Jordan, the Kingdom of Saudi Arabia, Korea, Laos, Malaysia, Myanmar, Pakistan, the Philippines, Singapore, South Africa, Thailand, Vietnam, Yemen and Kuwait. In terms of membership, GHWP is now the largest medical device regulatory harmonization body in the world. 

- Working model and structure: GHWP has an established technical and administrative work structure exemplified by a Technical Committee, seven  working groups and a special task group (pre-market submission and CSDT, IVDD post-market surveillance and vigilance, quality management system, quality system audit, clinical safety/performance, capacity building and regulatory training as well as medical device nomenclature) to focus on the development of the technical contents on various aspects of medical device regulatory affairs, towards harmonization among GHWP member economies.

- Link with the Global Harmonization Task Force (GHTF) and International Medical Device Regulator Forum (IMDRF): As a liaison body of the GHTF, GHWP works in coordination with the GHTF by participating in the GHTF Steering Committee and study groups contributing to the development of the GHTF guidance documents, promotion of understanding to the GHTF guidance documents and the facilitation on the adoption and adaptation of these guidance documents in the GHWP member economies. GHWP aims to work with IMDRF, successor to GHTF and custodian of the GHTF legacy, to keep guidance documents actualized. 

- International collaboration: Besides GHTF, GHWP has also established a connection with other international organizations, such as IMDRF WHO, ISO, IECAPEC, etc., to bring awareness of the needs and interests of GHWP to the global medical device arena. GHWP is also affiliated with the Committee of the newly formed IMDRF (International Medical Device Regulators Forum). GHWP will continue to work collaboratively with the related international organizations to achieve regulatory harmonization. GHWP recommend its members to have an active role in international standardization as one of the most powerful tools to achieve harmonization.

With all the previous achievements by GHWP, there are still many challenges and work to be done in future. Many GHWP members are developing economies with emerging medical device regulatory regimens. Regulators and industry members have limited experience and resources in implementing their medical device regulation. Meanwhile, medical technologies have been evolving rapidly, and playing a more and more important role in the healthcare service delivery.  The locus of invention and production of medical devices has become more geographically dispersed. There is a growing demand for technologies to enable the diagnostic tests and therapies to be better appropriate, accessible and affordable in less developed economies. Since many of these regulatory systems are still in the formative stages, there is great opportunity for the prospective of harmonization on the regulatory requirements and practices within GHWP member economies.

In November 2011, Saudi FDA took over the chairmanship of GHWP from China SFDA (2009-2011).  Under the new leadership, GHWP develops a Strategic Framework Towards 2020 with the theme on “The Foreseeable Harmonization Horizon”, to enable a clear development plan and work targets towards the further enhancement of the capability of GHWP member economies in regulating medical devices, as well as the further strengthening of medical device regulatory harmonization and collaboration activities across the regions.

Strategic Frame Work Towards 2020

The Strategic Framework Towards 2020: Foreseeable Harmonization Horizon serves as a guide for various GHWP activities, including: organizational presence and partnership, expansion, training and capacity building, and the regulatory convergence goal, which contributes to the achievement of GHWP’s mission: to promote regulatory harmonization in order to enhance patient safety and increase access to safe, effective and clinically beneficial medical technologies across GHWP member economies.

Potential indicators of success:
• Increased inclusiveness of GHWP membership, therefore the further expansion of regulatory and industry members from more economies to join GHWP and participate in GHWP activities, for the benefit of both the GHWP members and non-members.
• Enhanced awareness on the robust and efficient medical device regulation, to ensure improved access, quality and use of medical devices to healthcare policy makers, regulators, industry and other stakeholders throughout the GHWP member economies.
• Adoption or adaptation of the GHTF global regulatory model and the model of the other international harmonization bodies for the construction of the regulatory system by GHWP members. and expedite the  implementation of GHWP guidance which adopted or adapted from GHTF guidance in GHWP member economies, for example:
- The definition of : “medical device”, “manufacturer”, “authorized representative”, “distributor”, “importer”, and other terms as defined in GHTF guidance;   
- Registration of manufacturers, distributors, and importers and listing of medical devices;
- Risk-based classification of medical devices;
- Post market vigilance and surveillance framework;
- Medical device nomenclature system, etc.
• Enhanced collaboration among GHWP member economies, to improve and promote greater efficiency on regulation and the use of resources. For example: 
- Single nomenclature system;
- Convergence towards a single post-market surveillance framework;
Mutual acceptance of quality management system and auditing report, etc. Synchronization in the adoption of international safety standards
• Enhanced global partnership between GHWP and the other international organizations. For example:
- GHWP’s participation and representation at regional/global forums;
- Joint strategic planning, roadmap development, conference and activities with other regional and global organizations such as WHO, APEC, etc.

Framework Element One:  GHWP Membership Expansion

Medical device manufacturing is booming in many economies worldwide, that are not member economies of GHWP. At the same time, member economies of GHWP are developing new medical device regulations or revising their existing systems. Given the rising wave of interest in the international and cross-regional collaboration and harmonization of medical device regulation, the GHWP should reach out to non-member economies and form the alliances with economies and associations across the globe.

GHWP would continue to welcome any members who show interest in participating, even though they may have no, or only rudimentary, medical device regulatory regimes. Their participations can benefit patients, regulatory authorities and medical device industry through improved access to high quality, safe and innovative medical devices by understanding and adoption of  international best practices through GHWP training and capacity building, and by discussion on the development, adaptation, and adoption of the GHTF guidance documents.

Through the strategic set up of permanent secretariat office and legal entity in Hong Kong, GHWP is enabled to offer support to member economies with consistent and quality services through the secretariat office. GHWP has been offering necessary support to the member economies to regulatory authorities and industries in joining the GHWP meetings, workshops, conferences and events, which also strengthened our linkages and networks within member economies, creating good opportunities to narrow the gaps of medical device harmonization among member economies of GHWP.

While reaching out to non-member economies, it is equally important to invite economies  with experience and knowledge on medical device regulation to take the leading roles at various levels (GHWP, GHWP TC, working groups) in GHWP, so that their extensive experience and knowledge on medical device regulatory affairs, including the adoption and adaption of GHTF guidance, can be shared further.  Greater progress can be made through sharing of experience in improvement of practices and converging towards international best practices.

Framework Element Two: Training and capacity building  

The support on strategic elements of membership expansion, training and capacity building are extremely important to GHWP. These are important elements of promoting better understanding of international best practices on medical device regulation and contributing to achieving the ultimate goal of GHWP, and to achieve regulatory convergence towards international best practices. 

The objective of training and capacity building should be focused on helping regulators and the industry in understanding the medical device technology, the rationale behind medical device regulation and international best practices, thereby avoiding the mistakes that the other economies may have made, therefore to reduce the costs of re-inventing the wheel amongst GHWP member economies. For those GHWP member economies which have very limited resources and have no medical regulatory system in place, this training and capacity building should help healthcare policy makers, regulators, industry, healthcare professionals and other stakeholders to enhance their knowledge on medical devices, and to understand the most important and essential elements of medical device regulation.

GHWP has conducted training and capacity building activities over the years through its working groups, as well as the collaboration with other global organizations like APEC, GHTF, etc. Moving forward, GHWP shall look into a more systematic approach to the overall training plan.

As mentioned above, some current and prospective GHWP members have not yet established their medical device regimes. Most GHWP members have relatively very limited resources and experience on medical device regulation. GHWP would further offer support on training and capacity building to member economies through the resources of GHWP, in terms of financial and manpower in-kind support.

The training and capability building efforts should lead to the identification of priorities for regulatory system development, optimize the use of regulatory resources, and contribute to the ultimate goal of improved patient access to high quality, and safe medical devices.

GHWP will facilitate the process of building consensus among potential training partners from non-profit organizations, regional/global harmonization organizations (e.g. WHO, APEC, RAPS, MTLI, ARPA, etc.), universities, etc., to leverage on their expertise on the delivery of capacity training, to work with them in curriculum development on medical device regulations tailored for the needs of GHWP member economies.  Informative materials as in international standards will also be considered in the curriculum development. All training activities should be planned and reviewed periodically and serve the GHWP strategic goal of achieving regulatory convergence.

GHWP should actively promote the full utilization of advanced technologies in training, such as webcast, web seminar, on-line training, etc., in supplement of traditional workshops and conferences.

Framework Element Three: Harmonization in Key Areas based on GHTF Principles and GHWP guidance

Some GHWP member economies have not yet established their medical device regimes or are in the process of establishing their medical device regimes. Some of them are re-visiting their existing systems.

GHWP should identify important areas with the most potential for success in harmonization based on the availability of GHTF global regulatory model and GHWP guidance within the GHWP region, and work out a clear timeline. Based on the progress achieved in GHWP, the areas below should be considered for regulatory convergence in a defined time frame.

- Harmonized definition of the term "medical device" (important in determining what and who are subject to regulation);
- Registration of manufacturers, distributors, and importers and listing of medical devices marketed;
- Adopt similar Risk-based classification of medical devices;
- Single adverse event reporting and post-marketing surveillance system;
- Single medical device nomenclature system;
- Single quality management system requirements, and broader acceptance of  quality management system audit report by authorized competent authorities ;
- Acceptance of clinical evidence gathered, and evaluations conducted by, other GHWP/GHTF members  ;
- Acceptance of the same dossier (technical file) template for registration submission (e.g. the CSDT format);
- Recognition of ‘recognized regulatory agencies’ registration decisions to expedite evaluation process, etc.

Framework Element Four: Enhance GHWP’s Global Partnership

GHWP should proactively approach international/regional organizations (e.g. IMDRF, APEC, ASEAN, WHO), global leaders and experts, to identify important topics and to establish mechanisms for effective interaction and networking. This could include, but not be limited to:
• a process of receiving from and providing feedback  to these organizations;
• membership and representation at these organizations;
• joint strategic planning and roadmap development (especially in the areas of common interest and benefit)
• joint activities and events in promoting regulatory harmonization/convergence

All these partnerships would further enhance the extent of regulatory harmonization within the GHWP member economies.


This Strategic Framework is intended as a path forward for the GHWP, to build on its momentum from the past, to develop the strategic direction for the future development of GHWP, which includes working in alignment with the interests of APEC, ASEAN, GHTF and IMDRF to promote regulatory convergence to bring about faster market access through engagement of  all stakeholders, and achieve a wider understanding of the benefits of international harmonization so that member economies of GHWP can implement best practices in their national regulatory systems. GHWP intends to share its consideration with IMDRF in order to keep the legacy of GHTF guidance documents actualized Member economies of GHWP will be adequately prepared to achieve their goal this based upon the application of GHWP as a platform for training and capacity building, the confidence building with the use of harmonized standards and best practices, and the assurance of alignment of the direction of GHWP with other regional/global regulatory harmonization organizations.  This will ensure timely access of patients to the medical device and related new medical technologies based on the fundamental principles of safety and efficacy.