Towards a data transfer agreement for the South African research community: The empowerment approach

JurisdictionSouth Africa
Date01 April 2023
Pages13-18
AuthorL Swales,M Botes,D Donnelly,D Thaldar
Published date01 April 2023
DOI10.7196/SAJBL.2023.v16i1.827
April 2023, Vol. 16, No. 1 SAJBL 13
ARTICLE
In the scientific research context, it is trite that data are enormously
valuable in advancing solutions to various health problems.
Therefore, cross-border data transfers are increasingly becoming
the norm, rather than the exception. However, how should South
African (SA) data providers ensure that such data sharing is done on
fair terms, and that their reasonable interests are legally protected?
One apparent answer is a data transfer agreement (DTA). Typically,
a DTA is a written agreement that regulates the lawful transfer of
data between a provider and a recipient by setting out, inter alia: the
purpose of the agreement; the obligations on each party; the term,
ownership and intellectual property; and other critical boilerplate
legal provisions. But instructing an attorney to draft a DTA for every
data transfer transaction is an expensive exercise. Moreover, the
field of data protection is becoming increasingly specialised. There
is a myriad of local, regional and international laws that apply to
data transfers,[1] which makes it increasingly challenging for SA data
providers to comply with the law. Here, government – or any civil
society organisation – can assist by developing a top-quality DTA
template and making it available to the research community to use.
In this article, we firstly provide some background on the topic of a
DTA template for SA. We then engage with the fundamental question
of how such an envisioned DTA template should be operationalised.
We suggest a paradigm shift away from the regulatory approach
taken with the material transfer agreement (MTA) that the SA Minister
of Health promulgated in 2018 (SA MTA).[2] While the regulatory
approach entails a single ‘solution’ that is made mandatory for all, we
suggest an empowerment approach, on which we elaborate in this
article. We also make an initial foray into the content suitable for a
DTA template in the SA context.
Background
The idea of a national template to regulate data transfers containing
standard data protection provisions to assist the SA research
community is not a novel idea. Most prominently, in 2018, Mahomed,[3]
in her doctoral thesis, suggested that the material transfer agreement
(MTA) that she developed can be used nationally as a template.
This MTA included data-related provisions. Later the same year,
the SA Minister of Health promulgated the SA MTA – based almost
entirely on the MTA developed by Mahomed. The minister’s action
to promulgate the SA MTA was over-hasty and ill-advised. There
was no prior public consultation that could have proved essential in
ironing out issues with the SA MTA’s content. For example, the SA MTA
provides that once the agreement becomes effective, the material
that is the subject of the agreement is deemed to be transferred by
the provider and accepted by the recipient– irrespective of whether
the material was in fact transferred and accepted– hence creating
a potentially problematic legal fiction.[4,5] From a practical legal
perspective, this is an obvious issue that could have been pointed
out to the minister, had he only consulted before promulgating the
SA MTA. Furthermore, it has been highlighted in the literature that the
SA MTA is in conflict with other pieces of legislation administered by
the Minister of Health.[6-9]
This open-access article is distributed under
Creative Commons licence CC-BY-NC 4.0.
Towards a data transfer agreement for the South African
research community: The empowerment approach
L Swales,1 PhD; M Botes,1,2 LLD; D Donnelly,1 PhD, D Thaldar,1,3 PhD
1 School of Law, College of Law and Management Studies, University of KwaZulu-Natal, Durban, South Africa
2 SnT Centre for Security, Reliability and Trust, University of Luxembourg, Luxembourg
3 Petrie-Flom Center for Health Law Policy, Biotechnology, and Bioethics, Harvard Law School, Cambridge, USA
Corresponding author: L Swales (SwalesL@ukzn.ac.za)
The idea of a data transfer agreement (DTA) template for the South African (SA) research community is receiving increasing attention. While
developing such a DTA template is certainly a worthwhile project, questions regarding the project’s practical execution should be addressed,
including how to best operationalise the envisioned DTA template, and the content of the envisioned DTA template. It is proposed that an
empowerment approach be followed in operationalising the envisioned DTA template, which is contrasted with the regulatory approach
followed with the material transfer agreement that the Minister of Health promulgated in 2018. While the regulatory approach would entail
government making the use of the envisioned DTA template compulsory regardless of the quality of such a template, the empowerment
approach, by contrast, entails a focus on developing a high-quality, professionally drafted DTA template for the SA research community and
making the use thereof a matter of own choice. Regarding the content of the envisioned DTA template, four hot-button content provisions
are analysed, and it is argued that SA research institutions and researchers should be empowered to: (i) have clarity and legal certainty
regarding their ownership of data, where relevant; (ii) be able to commercialise their research findings without unnecessary contractual
constraints; (iii) avoid falling into the trap of unlawful benefit sharing with research participants; and (iv) be aware that their legal role as
responsible parties, where relevant, cannot be contracted out via a DTA.
S Afr J Bioethics Law 2023;16(1):e827. https://doi.org/10.7196/SAJBL.2023.v16i1.827

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