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Learn how GA4GH helps expand responsible genomic data use to benefit human health.
Learn how GA4GH helps expand responsible genomic data use to benefit human health.
Our Strategic Road Map defines strategies, standards, and policy frameworks to support responsible global use of genomic and related health data.
Discover how a meeting of 50 leaders in genomics and medicine led to an alliance uniting more than 5,000 individuals and organisations to benefit human health.
GA4GH Inc. is a not-for-profit organisation that supports the global GA4GH community.
The GA4GH Council, consisting of the Executive Committee, Strategic Leadership Committee, and Product Steering Committee, guides our collaborative, globe-spanning alliance.
The Funders Forum brings together organisations that offer both financial support and strategic guidance.
The EDI Advisory Group responds to issues raised in the GA4GH community, finding equitable, inclusive ways to build products that benefit diverse groups.
Distributed across a number of Host Institutions, our staff team supports the mission and operations of GA4GH.
Curious who we are? Meet the people and organisations across six continents who make up GA4GH.
More than 500 organisations connected to genomics — in healthcare, research, patient advocacy, industry, and beyond — have signed onto the mission and vision of GA4GH as Organisational Members.
These core Organisational Members are genomic data initiatives that have committed resources to guide GA4GH work and pilot our products.
This subset of Organisational Members whose networks or infrastructure align with GA4GH priorities has made a long-term commitment to engaging with our community.
Local and national organisations assign experts to spend at least 30% of their time building GA4GH products.
Anyone working in genomics and related fields is invited to participate in our inclusive community by creating and using new products.
Wondering what GA4GH does? Learn how we find and overcome challenges to expanding responsible genomic data use for the benefit of human health.
Study Groups define needs. Participants survey the landscape of the genomics and health community and determine whether GA4GH can help.
Work Streams create products. Community members join together to develop technical standards, policy frameworks, and policy tools that overcome hurdles to international genomic data use.
GIF solves problems. Organisations in the forum pilot GA4GH products in real-world situations. Along the way, they troubleshoot products, suggest updates, and flag additional needs.
NIF finds challenges and opportunities in genomics at a global scale. National programmes meet to share best practices, avoid incompatabilities, and help translate genomics into benefits for human health.
Communities of Interest find challenges and opportunities in areas such as rare disease, cancer, and infectious disease. Participants pinpoint real-world problems that would benefit from broad data use.
The Technical Alignment Subcommittee (TASC) supports harmonisation, interoperability, and technical alignment across GA4GH products.
Find out what’s happening with up to the minute meeting schedules for the GA4GH community.
See all our products — always free and open-source. Do you work on cloud genomics, data discovery, user access, data security or regulatory policy and ethics? Need to represent genomic, phenotypic, or clinical data? We’ve got a solution for you.
All GA4GH standards, frameworks, and tools follow the Product Development and Approval Process before being officially adopted.
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Help create new global standards and frameworks for responsible genomic data use.
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6 Jul 2020
The GDPR may apply to processing activities happening outside of Europe, commonly referred to as the GDPR’s “extraterritorial effect”. Reflecting the latest guidance on the subject from the European Data Protection Board (EDPB), this brief should be considered an update to an earlier brief on the GDPR’s territorial scope.
The GDPR may apply to processing activities happening outside of Europe, commonly referred to as the GDPR’s “extraterritorial effect”. Reflecting the latest guidance on the subject from the European Data Protection Board (EDPB), this brief should be considered an update to an earlier brief on the GDPR’s territorial scope.
The GDPR applies to processing activities rather than to individuals or organizations. This means that researchers and their institutions cannot accurately say that the “GDPR does not apply to us”. Rather, there are two principal criteria by which the GDPR may apply to the processing of personal data by organizations outside of the European Economic Area (EEA): the “establishment” criterion and the “targeting” criterion.
Establishment criterion
The GDPR applies to data processing activities occurring outside of the EEA that have a link to the activities of an establishment in the EEA. The notion of an “establishment” encompasses “any real and effective activity – even a minimal one – exercised through stable arrangements”. This may encompass processing activities carried out by a controller outside of the EEA but have a connection to an establishment within the EEA. For example, this would be the case where a pharmaceutical company based in the EEA has its research arm in Canada carry out its personal data processing activities related to genomics. While the Canadian office would not normally be within the territorial scope of the GDPR, the activities of the EEA establishment and their connection to the research arm draw the Canadian office into the establishment criterion.
Targeting criterion
Perhaps more far-reaching than the establishment criterion is the targeting criterion. Organizations should first ask themselves if the processing activities relate to the personal data of individuals in the EEA. Then if so, they should further ask whether processing relates to (1) the offering of goods and services or (2) the monitoring of behaviour of individuals in the EEA.
Offering goods and services may catch certain research projects depending on the circumstances: no payment is required and the return of results, for example, may qualify as a service. Monitoring the behaviour of EEA-based research participants may be more relevant for longitudinal studies or other research projects that are built upon participants habitually reporting their health status. Thus, for example, a research project based in Australia with a mobile app offered in the Benelux countries’ “app stores” that asks participants to periodically input their dietary and fitness information would be caught by the GDPR.
Concluding observations
An analysis of the GDPR’s applicability is a determination to be made on a case-by-case basis. Guidelines indicate that, for example, the merely incidental (non-intentional) processing of personal data of individuals in the EEA on its own is insufficient to trigger the GDPR’s application. Moreover, the mere selection of an EEA-based processor by a controller outside of the EEA, without other factors present, will not subject that controller to the GDPR. Frequently, however, the surrounding circumstances of personal data processing are not so simple and a determination may be difficult to make. Consequently, the EDPB’s guidelines on this subject are a “must read”. Finally, it should be noted that the European Commission has signalled its intention to further clarify the relationship between the GDPR’s territorial scope and its rules on data transfers outside of the EEA.
Further Reading
Relevant GDPR Provisions
Michael Beauvais works at McGill University’s Centre of Genomics and Policy.
See all previous briefs.
Please note that GDPR Briefs neither constitute nor should be relied upon as legal advice. Briefs represent a consensus position among Forum Members regarding the current understanding of the GDPR and its implications for genomic and health-related research. As such, they are no substitute for legal advice from a licensed practitioner in your jurisdiction.