Data Protection and Digital Information (No. 2) Bill (Second sitting)

Debate between Rebecca Long Bailey and Damian Collins

Committee stage
Wednesday 10th May 2023 Public Bill Committees

[Damian Collins]

Q I have a final question. We have this legislation, and then different tech companies and operating systems have separate guidelines that they work to as well. One of the issues the Government faced with, for instance, the covid vaccine app, was that it had to comply with the operating rules for Google and iOS, regardless of what the Government wanted it to do. Thinking of the work that your organisation has been involved in, are there still significant restrictions that go beyond the legal thresholds because different operating systems set different requirements?

Jonathan Sellors: I do not think I am really the best qualified person to talk about the different Android and Apple operating systems, although we did a lot of covid-related work during the pandemic, which we were not restricted from doing.

Tom Schumacher: I would say that this comes up quite a lot for Medtronic in the broader medtech industry. I would say a couple of things. First, this is an implementation issue more than a Bill issue, but the harmonisation of technical standards is absolutely critical. One of the challenges that we, and I am sure NHS trusts, experience is variability in technical and IT security standards. One of the real opportunities to streamline is to harmonise those standards, so that each trust does not have to decide for itself which international standard to use and which local standard to use.

I would also say that there is a lot of work globally to try to reach international standards, and the more that there can be consistency in standards, the less bureaucracy there will be and the better the protection will be, particularly for medical device companies. We need to build those standards into our product portfolio and design requirements and have them approved by notified bodies, so it is important that the UK does not create a new and different set of standards but participates in setting great international standards.

[Rebecca Long Bailey (Salford and Eccles) (Lab)]

Q In relation to medical research, concerns have been raised that the Bill might risk a divergence from current EU adequacy and that that might have quite a significant detrimental impact on collaboration, which often happens across the EU on medical research. Are you concerned about that, and what should the Government do to mitigate it?

Jonathan Sellors: I think that it is absolutely right to be concerned about whether there will be issues with adequacy, but my evaluation, and all the analysis that I have read from third parties, particularly some third-party lawyers, suggests that the Bill does not or should not have any impact on the adequacy decision at all—broadly because it takes the sensible approach of taking the existing GDPR and then making incremental explanations of what certain things actually mean. There are various provisions of GDPR—for example, on genetic data and pseudonymisation—that are there in just one sentence. It is quite a complicated topic, so having clarification is thoroughly useful, and I do not think that that should have any impact on the adequacy side of it. I think it is a very important point.

Tom Schumacher: I agree that it is a critical point. I also feel as though the real value here is in clarifying what is already permitted in the European GDPR but doing it in a way that preserves adequacy, streamlines and makes it easier for all stakeholders to reach a quick and accurate decision. I think that adequacy will be critical. I just do not think that the language of the text today impacts the ability of it to be adequate.