Tag Archives: Siobhan Green

How to Develop and Implement Responsible Data Policies

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A friend reminded me at the MERL Tech Conference that a few years ago when we brought up the need for greater attention to privacy, security and ethics when using ICTs and digital data in humanitarian and development contexts, people pointed us to Tor, encryption and specialized apps. “No, no, that’s not what we mean!” we kept saying. “This is bigger. It needs to be holistic. It’s not just more tools and tech.”

So, even if as a sector we are still struggling to understand and address all the different elements of what’s now referred to as “Responsible Data” (thanks to the great work of the Engine Room and key partners), at least we’ve come a long way towards framing and defining the areas we need to tackle. We understand the increasing urgency of the issue that the volume of data in the world is increasing exponentially and the data in our sector is becoming more and more digitalized.

This year’s MERL Tech included several sessions on Responsible Data, including Responsible Data Policies, the Human Element of the Data Cycle, The Changing Nature of Informed Consent, Remote Monitoring in Fragile Environments and plenary talks that mentioned ethics, privacy and consent as integral pieces of any MERL Tech effort.

The session on Responsible Data Policies was a space to share with participants why, how, and what policies some organizations have put in place in an attempt to be more responsible. The presenters spoke about the different elements and processes their organizations have followed, and the reasoning behind the creation of these policies. They spoke about early results from the policies, though it is still early days when it comes to implementing them.

What do we mean by Responsible Data?

Responsible data is about more than just privacy or encryption. It’s a wider concept that includes attention to the data cycle at every step, and puts the rights of people reflected in the data first:

  • Clear planning and purposeful collection and use of data with the aim of improving humanitarian and development approaches and results for those we work with and for
  • Responsible treatment of the data and respectful and ethical engagement with people we collect data from, including privacy and security of data and careful attention to consent processes and/or duty of care
  • Clarity on data sharing – what data, from whom and with whom and under what circumstances and conditions
  • Attention to transparency and accountability efforts in all directions (upwards, downwards and horizontally)
  • Responsible maintenance, retention or destruction of data.

Existing documentation and areas to explore

There is a huge bucket of concepts, frameworks, laws and policies that already exist in various other sectors and that can be used, adapted and built on to develop responsible approaches to data in development and humanitarian work. Some of these are in conflict with one another, however, and those conflicts need to be worked out or at least recognized if we are to move forward as a sector and/or in our own organizations.

Some areas to explore when developing a Responsible Data policy include:

  • An organization’s existing policies and practices (IT and equipment; downloading; storing of official information; confidentiality; monitoring, evaluation and research; data collection and storage for program administration, finance and audit purposes; consent and storage for digital images and communications; social media policies).
  • Local and global laws that relate to collection, storage, use and destruction of data, such as: Freedom of information acts (FOIA); consumer protection laws; data storage and transfer regulations; laws related to data collection from minors; privacy regulations such as the latest from the EU.
  • Donor grant requirements related to data privacy and open data, such as USAID’s Chapter 579 or International Aid Transparency Initiative (IATI) stipulations.

Experiences with Responsible Data Policies

At the MERL Tech Responsible Data Policy session, organizers and participants shared their experiences. The first step for everyone developing a policy was establishing wide agreement and buy-in for why their organizations should care about Responsible Data. This was done by developing Values and Principles that form the foundation for policies and guidance.

Oxfam’s Responsible Data policy has a focus on rights, since Oxfam is a rights-based organization. The organization’s existing values made it clear that ethical use and treatment of data was something the organization must consider to hold true to its ethos.

It took around six months to get all of the global affiliates to agree on the Responsible Program Data policy, a quick turnaround compared to other globally agreed documents because all the global executive directors recognized that this policy was critical.

A core point for Oxfam was the belief that digital identities and access will become increasingly important for inclusion in the future, and so the organization did not want to stand in the way of people being counted and heard. However, it wanted to be sure that this was done in a way that balanced and took privacy and security into consideration.

The policy is a short document that is now in the process of operationalization in all the countries where Oxfam works. Because many of Oxfam’s affiliate headquarters reside in the European Union, it needs to consider the new EU regulations on data, which are extremely strict, for example, providing everyone with an option for withdrawing consent.

This poses a challenge for development agencies that normally do not have the type of detailed databases on ‘beneficiaries’ as they do on private donors. Shifting thinking about ‘beneficiaries’ and treating them more as clients may be in order as one result of these new regulations. As Oxfam moves into implementation, challenges continue to arise.

For example, data protection in Yemen is different than data protection in Haiti. Knowing all the national level laws and frameworks and mapping these out alongside donor requirements and internal policies is extremely complicated, and providing guidance to country staff is difficult given that each country has different laws.

Girl Effect’s policy has a focus on privacy, security and safety of adolescent girls, who are the core constituency of the organization.

The policy became clearly necessary because although the organization had a strong girl safeguarding policy and practice, the effect of digital data had not previously been considered, and the number of programs that involve digital tools and data is increasing. The Girl Effect policy currently has four core chapters: privacy and security during design of a tool, service or platform; content considerations; partner vetting; and MEAL considerations.

Girl Effect looks at not only the privacy and security elements, but also aims to spur thinking about potential risks and unintended consequences for girls who access and use digital tools, platforms and content. One core goal is to stimulate implementers to think through a series of questions that help them to identify risks. Another is to establish accountability for decisions around digital data.

The policy has been in process of implementation with one team for a year and will be updated and adapted as the organization learns. It has proven to have good uptake so far from team members and partners, and has become core to how the teams and the wider organization think about digital programming. Cost and time for implementation increase with the incorporation of stricter policies, however, and it is challenging to find a good balance between privacy and security, the ability to safely collect and use data to adapt and improve tools and platforms, and user friendliness/ease of use.

Catholic Relief Services has an existing set of eight organizational principles: Sacredness and Dignity of the human person; Rights and responsibilities; Social Nature of Humanity; The Common Good; Subsidiarity; Solidarity; Option for the Poor; Stewardship.

It was a natural fit to see how these values that are already embedded in the organization could extend to the idea of Responsible Data. Data is an extension of the human person, therefore it should be afforded the same respect as the individual. The principle of ‘common good’ easily extends to responsible data sharing.

The notion of subsidiarity says that decision-making should happen as close as possible to the place where the impact of the decision will be the strongest, and this is nicely linked with the idea of sharing data back with communities where CRS works and engaging them in decision-making. The option for the poor urges CRS to place a preferential value on privacy, security and safety of the data of the poor over the data demands of other entities.

The organization is at the initial phase of creating its Responsible Data Policy. The process includes the development of the values and principles, two country learning visits to understand the practices of country programs and their concerns about data, development of the policy, and a set of guidelines to support staff in following the policy.

USAID recently embarked on its process of developing practical Responsible Data guidance to pair with its efforts in the area of open data. (See ADS 579). More information will be available soon on this initiative.

Where are we now?

Though several organizations are moving towards the development of policies and guidelines, it was clear from the session that uncertainties are the order of the day, as Responsible Data is an ethical question, often relying on tradeoffs and decisions that are not hard and fast. Policies and guidelines generally aim to help implementers ask the right questions, sort through a range of possibilities and weigh potential risks and benefits.

Another critical aspect that was raised at the MERL Tech session was the financial and staff resources that can be required to be responsible about data. On the other hand, for those organizations receiving funds from the European Union or residing in the EU or the UK (where despite Brexit, organizations will likely need to comply with EU Privacy Regulations), the new regulations mean that NOT being responsible about data may result in hefty fines and potential legal action.

Going from policy to implementation is a challenge that involves both capacity strengthening in this new area as well as behavior change and a better understanding of emerging concepts and multiple legal frameworks. The nuances by country, organization and donor make the process difficult to get a handle on.

Because staff and management are already overburdened, the trick to developing and implementing Responsible Data Policies and Practice will be finding ways to strengthen staff capacity and to provide guidance in ways that do not feel overwhelmingly complex. Though each situation will be different, finding ongoing ways to share resources and experiences so that we can advance as a sector will be one key step for moving forward.

This post was written with input from Maliha Khan, Independent Consultant; Emily Tomkys, Oxfam GB; Siobhan Green, Sonjara and Zara Rahman, The Engine Room.