Good morning and welcome to the 17th meeting in 2014 of the Health and Sport Committee. As usual at this point, I ask everyone in the room to switch off mobile phones and other wireless devices, because they can interfere with the sound system. I point out to our panellists that some members and officials are using tablet devices instead of hard copies of their papers.
Good morning, everybody. Will food standards Scotland merely take over the functions and administrative responsibilities of the Food Standards Agency, or will its doing so mean any benefits either financially or to the health and wellbeing of the Scottish people?
Perhaps I can explain the role of the Scottish Food Advisory Committee, which I chair. The committee is part of the Food Standards Agency, which is a United Kingdom body, and it inputs information on interests in Scotland to the deliberations of the UK board. I chair that committee and I also sit on the FSA board. We look at all the papers that come for decisions at the UK board and we offer Scottish input. The committee is part and parcel of the FSA.
Okay. Thank you.
We think that this is a real opportunity to create a strong new body that will be a consumer champion, so it should be about much more than just a transfer of administrative responsibilities. We campaigned for the setting up of the Food Standards Agency, which was to put consumers first and was to operate openly and transparently. However, some of the responsibilities of the Food Standards Agency in England have been taken away, which was one of the reasons for reviewing whether there should be a separate agency in Scotland.
Thank you. I have another question. Scotland is a significant food producer and we have a big processing interest. During the most recent foot-and-mouth disease outbreak, there was a concern among processors and producers that they were being unfairly treated, given that Scotland was free from the disease. Would the new agency have the powers to take a different line if something similar happened? If the opposite happened—if the incident was peculiar to Scotland and did not affect any other part of the United Kingdom—would the other parts of the UK be able to act differently, or would that be a step further than what is proposed?
What you suggest would be true in the sense that, with food standards Scotland, decisions would be made in Scotland. However, bugs do not observe borders and there would need to be very close liaison with the rest of the UK about the arrangements. That, in itself, would—I hesitate to say “limit”—influence the policy and the actions that would be taken on things such as foot-and-mouth disease. Food standards Scotland would need to take those arrangements very seriously and co-ordinate its actions very closely with the rest of the UK to fight foot-and-mouth disease and other infectious diseases. That collaboration will be essential in the future, even with the separate body in Scotland.
I certainly emphasise the point that bugs do not recognise boundaries, so a collaborative approach will be needed on some major issues.
I agree with Jim Wildgoose’s point about bugs not stopping at the border. It will be important to consider issues case by case. It may be appropriate and possible for Scotland to take a different approach on some issues, but the way that the agency works will have to be seen in the context of what happens throughout the UK and how possible it is to put controls in place, as well as in the wider EU context, because much will be decided by EU legislation.
I agree entirely with Dr Jim Wildgoose. When I was visiting China—it was nothing to do with food, but my company does business in China—I was amazed that people approached me about the “Scottish” label. They were interested in purchasing because the food is so trustworthy, not because of what they perceived the quality to be.
What will the bill achieve? We heard in a private briefing this morning that the regulation and standards are already in place to monitor foot-and-mouth disease, and that enforcement will lie outwith the agency, with local authorities or supermarket chains, as we heard yesterday, where inspection is much more rigorous. How will the bill enhance any of those functions when the aim is to reassure people that nothing much will change and we will still be plugged into the research and sharing of information? What is the point of the bill?
That is a fair question, but there are clear reasons why we have a separate bill and a separate agency.
I suppose that that is the question that we are asking now, as we did yesterday. What would we do differently? We were told earlier today in a private briefing that Scotland already has the powers to change labelling. If we wanted to change labelling, we could do it now.
Strictly speaking, that is correct, but responsibility currently lies with the FSA, which is the agency that is giving the advice. There will be a change and the new body in Scotland will give the advice. As the convener said, the legislative position is that those things are devolved and that decisions can be taken, but it would be the new body that would give the advice rather than the FSA.
Would we be more likely to do something on labelling?
Yes—we would be able to take our own decisions on labelling. The advice that will be given will be unashamedly Scottish advice, rather than UK advice.
That relates to evidence that we took yesterday about concern among manufacturers that we might have a labelling regime that is different from the regime in the rest of the UK.
This comes back to co-ordination with others. It is not right to think that we will end up making a whole lot of different decisions. We need to co-ordinate and ensure that the decisions that we make are the right ones and do not hamper industry. There will be certain areas in which we might want to do things slightly differently.
Would Sue Davies like to comment on the idea of a consumer-led food standards agency?
That is the key thing. We have an opportunity to ensure that we have a strong consumer champion, and that we have an agency that sets the benchmark for how other agencies should operate. We think—this is also one of the recommendations of the first Scudamore report—that it is important to have food safety, nutrition and standards in one place. As Jim Wildgoose mentioned, since the horsemeat scandal, it has become clear that food standards issues have not been getting enough attention and need to become a greater priority. We also see nutrition as an area in which there is a problem across the UK. Scotland has high rates of obesity and diet-related disease. The issue is complex: giving the new agency the ability to do work on it would be an advantage.
The convener raised an important point about differences that might arise in terms of labelling requirements or legislative requirements in different parts of the United Kingdom. The Scudamore panel, however, went out of its way to emphasise the importance of continuing collaboration, so where are the opportunities for that to happen? With regard to my sector, the meat inspection service is an integral part of the Food Standards Agency and there are opportunities to tailor it to the needs of the Scottish processing industry and to ensure that it delivers an efficient and effective service. Within the industry, there is a view that that would be positive and worth while.
From our visits yesterday, I understood that Scotland has led the way on the changes of labelling that are being implemented, and that the rest of the United Kingdom followed Scotland’s decision to change labelling. Is that correct, or were we given the wrong information?
I am not sure about the detail of the issue that you refer to. There is some leeway for separate decision making in Scotland, but I do not know the detail of that. All the labelling legislation is EU based, so the ground rules are set in Brussels. There are some derogations and opportunities for change that member states can make use of. I suspect that that is what you are referring to, so I do not think that there is an inconsistency, as such. However, it is not possible to make wholesale changes to labelling that would go against what the EU legislation says, and neither are there huge variations that can be made from that legislation.
And that will not change because of the legislation that we are considering.
No, it will not change.
On nutrition and health promotion, you said that food standards Scotland could lead the way on health-related issues such as obesity. However, that work falls within the remit of local government and NHS boards. What is in the bill to ensure that those organisations work together? It seems to me that the proposal could simply bring another layer into an area in which a number of agencies are all trying to do the same work. How would food standards Scotland interact with those bodies to ensure that they are all singing from the same hymn sheet?
The answer lies in the question itself. A huge number of bodies are involved in this area and, although we know a lot about what to do with nutrition, I and, indeed, SFAC believe that we need co-ordination and that we get away from the kind of initiativitis—to coin a word—where we have initiative after initiative that might all be good in themselves but which, in my judgment, lack leadership and co-ordination. Various people have provided evidence of that, and SFAC has been dealing with the matter.
It is important that lots of co-ordination mechanisms are in place for different groups. For example, food standards Scotland will have to be very collaborative in how it works with other groups. One of the key issues will be to ensure that its board has strong consumer and public health representation so that it can send out a strong signal about what it is about and make it clear that it is not an industry promotion body. After all, other bodies have that responsibility.
Do you think that the powers to provide leadership in this area are missing from the bill, or will that sort of thing have to be set up in memorandums of understanding, through working together and so on? I cannot see how food standards Scotland can take leadership in an area where others have a statutory responsibility unless it is empowered to do so.
I am expressing a personal view but, as you have pointed out, we will need collaboration, memorandums of understanding, service level agreements and various such things to bring people together and take hold of the issue on a national basis. Quite a lot can be achieved by bringing people together. I accept that statutory responsibility lies elsewhere, but I do not think that that situation needs to change for us to achieve a better, focused approach. If you sought to change the responsibility, that could be a fundamental change, but I am not sure that it would generate the kind of change that you would want.
The proposed new body needs to take a leadership role. Its powers to operate openly and transparently and to publish the advice that it gives will be really important in that regard. It is also important that it plays a strong role, sets out exactly what action it expects to be taken and uses its powers to name and shame and to highlight who is and is not taking that action. Even if it does not have the ability to legislate, it can still deliver change across the whole industry.
Does anyone have any other comments on this? Do we have evidence regarding the board and the composition of its membership? Sue Davies mentioned that subject.
I will comment generally. Reference has been made to having the right structure and the right representation on the board, including health representation and consumer representation. It is important to have appropriate food sector representation on the board, too, so that a general understanding of how the industry operates can be taken to the table. All of that is underpinned by putting consumer interests first. It is important that the board is as widely based as possible in its views and experience. Perhaps the maximum number of seven should be considered a bit further.
I, too, was wondering about seven being the maximum number of members. There is no definitive answer, but that number seemed a bit on the low side.
That is important. It would be dangerous to start to have different industry sectors represented on the board promoting their own particular interests. That would move the new body away from the public health and consumer focus that it needs to have. It should be clearer in the bill that members of the board are there to act in the public interest, and that they should not have any conflicts of interest. That does not mean that they do not have relevant experience and skills but, overall, and as Jim Wildgoose said, they should be there to act together in the public interest.
It is helpful that the convener has picked up on some of the corporate governance issues, as that allows me to move on to the nuts and bolts of the bill. As an aside, it would be useful for us to get a brief note—perhaps not in this evidence session—on food safety standards with regard to traceability, welfare and other such things. As the European elections have just finished, it would be good to see the positive role that the European Union can play. It is important to put that on the record as an issue for another day.
The good thing about the bill is that it will extend many of the provisions that currently apply to food safety to cover what it terms “food information.” As you say, that will include the power to seize products that are not labelled properly and are misleading or fraudulent.
Convener, do you mind if I ask a supplementary on that specific point before the other two witnesses come in?
No, go on.
Would the duty to disclose food industry testing be a standard duty? Would it be imposed by a sheriff who was dealing with an issue through the courts? How would it work?
The problem that arose with horsemeat was that the Food Standards Agency did not, when it realised that there was a problem, have the power to enter many of the premises or require the food industry to carry out testing. The agency managed to get a voluntary agreement with the food industry to do more testing. The provision in the bill would apply in that type of situation to ensure that, when food standards Scotland needed the industry to carry out testing, that would be done. I would assume that, if such testing was not done, it would be a criminal offence.
That is very helpful.
The detail would be for the lawyers, but my understanding is similar to that of Sue Davies. The provisions that currently apply to food safety under the Food Safety Act 1990 will apply to food standards too.
That is helpful. Mr Donaldson, do you have anything to add?
I have nothing to add to that. That has covered it comprehensively.
I would like to clarify something. Are there examples of cases in which food information or labelling has been wrong, where authorities have stepped in and seized the food, and where they have wanted to ensure that that food was not put back into the consumer food chain, even though it was safe—just a case involving wrong food information or food fraud—but where the food still re-entered the world of the consumer? The policy memorandum suggests that that is a possibility as the law stands, because sheriffs do not have the power to keep the food. Is it currently the case that, if they seize the food and it is perfectly safe and not breaking any laws other than food information or food fraud laws, it has to be returned? I found it quite staggering that the policy memorandum suggests that, and I want to be clear about the situation.
It is my understanding that there is a gap in the legislation. I am not a lawyer and I have not looked at the matter in great detail, but that is my understanding of the position. The detail would need to be checked with the lawyers, but I am pretty sure that the memorandum will have been produced by lawyers and that it will reflect the current position.
That is fine. When we come to the nuts and bolts of the bill, we find that the bill creates a duty that does not exist at the moment to report breaches of food standards or food information requirements. If you run a small business and seek to enter into an agreement to get some food produce, and then you find out that it is not legit, there has not been a duty on you to report that to the relevant authorities. A good small business would walk away and deal with a legitimate supplier, but it would not be compelled to report the breach. That compulsion is now contained in the bill, and it will be an offence not to report such a breach. Is that a provision that all three of you are content with?
Yes, we are pleased that that is in the bill. It makes it clear that standards are an important issue. It came out in the Scudamore report, and Elliott’s interim report on horsemeat has also highlighted concerns about a culture of turning a blind eye in the industry globally. People have been buying ingredients at prices that could not possibly be realistic, and the introduction of standards can start to change that culture and make it clear that fraudulent practices are unacceptable.
I take it that the other witnesses have nothing else to add.
I think that there are a couple of supplementary questions on that point.
One thing that was suggested to us on our visit yesterday was that the ability to fine or punish somebody for fraud is really quite inadequate relative to the profits that are being made through criminal activity. Does the bill, or might the regulations, provide the scope to ensure adequate punishment of criminal activity that is highly profitable?
That is being debated at EU level. The European Parliament has been considering the official controls regulation, which will be finalised when the new Commission and Parliament come back in the autumn. The Commission proposed that the fine should be equivalent to the cost of the financial gain from the criminal activity, but the Parliament has suggested that it should be double the financial gain, which we support. We need a range of enforcement tools. The fixed penalty notices will help, as will the requirement to disclose cases of fraud but, ultimately, there needs to be a criminal route as well as tough penalties. As I understand it, that measure would be reflected in the bill, but it is important that the provision is in it.
I have nothing much to add to that. It is generally recognised that the financial penalties in the area of food are much lower than those for contraventions outside that area, which can be punitive. As Sue Davies says, the issue is being considered at EU level to see what penalties are appropriate. I expect that things will change, depending on decisions in the EU.
We are thinking about the nuts and bolts and we are trying to ascertain whether there is general support or whether you have concerns. I am glad that there is support in relation to the duty to report non-compliance. The bill uses the terminology of “food business operator”. Are you content with the scope of that? Are there other people who might be aware of non-compliance and who would not have a duty to report but who should have such a duty? Many years ago, I was a kitchen porter in a hotel—earning peanuts, frankly. I would not want to put minimum wage staff in catering kitchens in an invidious situation by giving them a duty to report. Of course, there is a balance to be struck.
I see that Mr Donaldson’s microphone light is on.
Oh, right—I was not aware that it was on. I am not sure that I am the best person to answer that. It is appropriate that food business operators take responsibility for their actions—I do not think that anybody would disagree with that.
The term “food business operator” is a well-defined term in legislation. It is the responsibility of the food business operator to ensure safe food and food of a certain standard. To be honest, I had not thought further than that and considered who else might be involved, but there are ideas for things such as whistleblowing arrangements. Those are more the kind of issue that would be dealt with in a code of practice or through a standard approach. There are plenty of examples of things such as secure phone lines, which are the kind of thing that I would expect FSS to consider—actually, I think that the FSA is considering whistleblowing, which I think is the issue that Bob Doris is referring to. However, it would be dangerous to change the definition of the term, as it is central to the way in which the legislation works.
Bob Doris raises a good point. It is worth checking that nobody important would be excluded. With the horsemeat incident, all these brokers suddenly emerged that people had not necessarily been aware of. It would be good to ensure that all the intermediaries are covered by the definition of “food business operator”.
That is helpful.
The Scottish Food Advisory Committee has an input to the United Kingdom Food Standards Agency. Will the SFAC continue after the creation of the new body?
The simple answer is no. It will cease on the vesting day of the new body and the arrangements that you are talking about will cease. Those arrangements were set up to allow a Scottish input to UK decisions on food safety and will be taken over wholly by the FSS following vesting day.
I realise that the Food Standards Agency Scotland is a subsection of the old Food Standards Agency in the UK, so we needed the separate body to make that input. Will the new FSS have the opportunity to make that input?
Yes. It is worth saying that the Food Standards Agency Scotland is simply the Scottish executive end of the FSA, so all its line management and so on comes from FSA central headquarters. After vesting day, FSS will be an entirely separate and self-contained body. The arrangements that we have had hitherto have simply been about looking after Scottish interests within the UK setting.
Presumably then the FSS will take evidence from Rowett, the Cambridge unit, the Norwich unit, and elsewhere. How can we be sure that the evidence will be compiled in a suitable way? It is all about relationships. Will we still have access to Norwich and Cambridge? I understand that they are complementary to the Rowett. Are they the only bodies?
No. This is a fundamental point. A number of scientific advisory committees are UK based but also report to Scottish, Welsh and Northern Irish ministers. They cover the whole gamut of food safety and some go beyond that; some of them have a food remit along with other remits. They are standard scientific advisory committees that are charged with providing the Food Standards Agency with the best scientific advice that they can get. When issues arise that require scientific advice, they will frequently provide it.
I do not have much to add to that. It is important that there is a clear agreement about how that will operate to ensure that the existing scientific committees pick up Scotland-specific issues. The new food body might have to set up its own committees on particular issues, in which case we would want it to work in the same way as the FSA has worked—it ensures that it meets in public, and there are strict criteria around independence. Particularly as a lot of universities now rely on food industry funding for the research that they do, we need to ensure that the independence of the research is not compromised and that there is no perception of that.
Thank you. We are considering the bill at a difficult time, in the sense that, after 18 September, we might be independent. I wonder whether the bill would have to be adjusted even further or what would happen in the event of independence. How would we link into the systems, which are quite integrated at present?
That is a nice question and an important one. It would be quite a difficult and costly process to duplicate the 12 or 15 committees of key experts who sit and pronounce on a range of scientific issues. That is why it is important for FSS to latch on to them.
It is Public Health England.
Yes—I got that wrong. That means that it does not meet in public—it is internal. There might be a specific issue about that committee in Scotland. The issue really boils down to how the new body would work with the access that is available, given how significant nutrition is likely to be for the new body.
A lot of advice now comes from the European Food Safety Authority, which is the basis for a lot of European Union legislation, approvals of particular types of products and the setting of safe levels for chemical contaminants. A close relationship with it is important. Obviously, that will change, depending on what happens in September. Relationships with other bodies, such as the World Health Organization, will also be important.
I endorse that. It is an important point, which will require real consideration to ensure that we can find the best way forward and one that enhances food standards Scotland’s role.
In the consultation, respondents to the call for evidence raised the issue of the new body being properly resourced. Yesterday, issues were raised about the current situation, irrespective of what happens on 18 September. Issues were raised to do with the science, which I think has been covered; the direction and funding of research; who would decide the priorities; relationships with the Rowett and others; and how we would get a balance there. Are there any views on that in respect of resources? The budget that was mentioned yesterday was around £11 million, I think. Around £5 million is currently being negotiated back from the UK body. The new body will have an influence in and be a focus for the whole area and we are talking about it having a budget of around £16 million.
The whole area of research, access to research and research commissioning will need to be looked at very carefully for the new body. We in the SFAC have done a little bit of work on that to give to those who will be involved in constructing the new arrangements. There will need to be a mechanism for linking into Scotland-based scientific advice, and that will need to be done fairly carefully if access to the main scientific advisory committees continues, as we would not want competing advice. I see a role for that and for perhaps setting up a separate committee in Scotland. I notice that the bill allows for the construction of separate committees, for example. That is right, as there are other areas in which that approach might be important, as well.
The research budget may look small. I was a board member of Quality Meat Scotland, which had a research budget of around £300,000, but it attracted additional funding from the Scottish Government and other sources, including European sources. There are plenty of mechanisms to build on the core funding and for being led by the scientific needs and securing funding through those particular routes.
Collaboration will be important, where it is possible—in many areas, there will be only a limited number of experts to draw on. It is important that the source of the funding is clear, particularly in more controversial areas such as new food technologies, where one needs to ensure that one is relying on independent research.
I am interested in the point made by Mr Donaldson and Dr Wildgoose that there are individual budgets in different compartments, if you like, of different departments. Do we have any idea what the global figure is? The health service is looking at all this and is spending some money on research in relation to obesity, for example. The Food Standards Agency is doing likewise, as are others. Is there a global figure that could probably be used more effectively to focus on significant problems in Scotland?
I do not have a figure. I am not sure whether one exists somewhere—it may well do. However, I can tell you that there is a huge programme going on at the moment on E coli, which is a very important organism for Scotland. We tend to have a much larger incidence of shedding of E coli from cattle than elsewhere in the world, and certainly in comparison with the rest of the UK. A big programme on that is going on and a lot of Scottish Government money is going into it—it is not just FSA money. There might be research council money in it, too. I envisage collaborations being brought together to look at issues that are important for Scotland. You could envisage that kind of thing being important for the shellfish industry, which is important for Scotland, and perhaps for other areas. It all boils down to how food standards Scotland would take that agenda forward.
The issue is not just the sum of money that would be available, but the independence of the research, which Sue Davies referred to. Some general concerns about that were raised. Do you have any comments on that?
That is a perfectly sensible comment. It underlines the importance of FSS being independent and transparent. Funding sources should be very clear; I do not think that anybody would have an issue with that.
I am sorry for coming back to this so often, but one of the UK committees is the General Advisory Committee on Science, which is a new development from the past five or six years. GACS looks at issues to do with the arrangements of science, such as the use of industry-led data and so on; it has done work on that kind of thing. I am not aware of it having done any work on access to funds through industry, but it performs quite an important procedural role to do with how these things would work across the scientific advisory committees and research establishments. That is quite an important role for addressing the very question that you raise about industry money coming in in certain areas and the use of industry data, too.
Who would decide the priority in the budget? Would it be the board? Would there be influence from Government?
The General Advisory Committee on Science has tended to produce guidelines or procedures for use in particular areas. The one that I remember is on the use of data from other industry sources and how it can be best handled in research so that that is seen to be independent and objective.
Are you all satisfied that the bill will ensure independence, or will that be done through memoranda?
A lot of that is to be left to be sorted out at the next stage, through memoranda. That is why I said that the bill needs to be more explicit on issues such as the board’s make-up and avoiding conflicts of interest, although more general requirements on ethics in public life, for example, will apply.
Dr Wildgoose gave a balanced answer about how the best scientific advice is obtained when it is necessary. He said that the pre-eminent person or committee with the advice is approached, irrespective of whether that is for Scotland, the rest of the UK or Europe. The more I heard about funding, whether it is via the Scottish Government, UK research councils or Europe, the more I became—dare I say it—slightly excited, if that is the right expression, about the opportunities that are out there.
It will be important that food standards Scotland is linked in and takes opportunities where it can. As Jim Wildgoose said, lots of the same discussions are happening in lots of places. For example, the European Commission had a workshop a couple of weeks ago on tackling campylobacter, which is still the main type of food poisoning, and the Food Standards Agency will have a workshop on that next week. When the same experts are looking at different issues, it is important to work together.
The answer to the questions that Bob Doris posed is yes. FSS could have a role in leading the curve on certain issues. That will boil down to how FSS works, which is not an issue for the bill. The body will need to choose the issues that it is involved in, because it will not be able to do everything, but it could be seen to be promoting excellence in certain areas.
I was going to ask about horizon 2020, as I will return to our relationship with the European Union. I know that that is not part and parcel of the bill, but that relationship is important, given that much legislation on food policy comes from the EU. What percentage of the legislation that the FSA deals with comes from the EU? How do you see the new body developing or enhancing the relationship with EU institutions—not just the Commission and the Council but the European Parliament, which plays an important role as it is a co-legislator with the Council on a lot of food safety legislation?
Pretty much all food safety and food labelling legislation is decided at European level, but there is a certain amount of flexibility in implementation. The food information to consumers regulation, which was adopted a couple of years ago, is a big piece of food labelling legislation that covers everything from country of origin labelling and the labelling of meat products to nutrition labelling; the traffic light labelling scheme, which is voluntary, was developed after that came out. There is also slight flexibility around, for example, the amount of meat in sausages and pies and the retention of some of those reserve descriptions, but generally all the decisions are made at European level.
I agree entirely. More than 90 per cent of the legislation in question will be EU based. However, you will be aware of how policy gets developed in the EU; ideas float around Brussels and Luxembourg for a long time before they actually become legislation, and the process offers an opportunity to influence matters. Indeed, in our response to the consultation exercise, we suggested having secondments from the body in Scotland to the European institutions. We believe that being on the spot is really important in how those discussions move forward and in being able to influence things, and we feel that a more or less formalised approach to secondments will be very important if the body is not only to influence the debate but simply to get information back about what is going on and where the key issues lie. That links back to Sue Davies’s comment about having the right memorandums of understanding and SLAs.
Secondments are a very good idea, but we also need access to all the relevant advisory and scientific committees not just at a UK level but in the EU.
Indeed. The same point applies.
Richard Lyle will ask the next and final question.
This is not a question, just a comment. Dr Wildgoose said that bugs know no borders so, whatever happens in September, I am sure that the English and Scottish agencies will work with each other.
Yes, we said that. It was based on some research that we did, which we published in January.
That is an important issue as well. I keep saying that there are important issues, but the linkage is important because the vast majority of businesses that require regulation are regulated through local authorities. Although it is the local authorities’ responsibility, there is a kind of overall responsibility to Scotland to ensure that the legislation is complied with.
There is a lot of surveillance inspection on food hygiene and so on, but NHS Lothian made the point that there is no dietary surveillance. Perhaps there should be a role in that for the new body. What is your view on that? Is that a function of the FSA? If so, why will it not be transferred?
Some good information is already available under various surveys. They tend to be done on a UK basis, and Scotland sometimes augments the sample to get better information. That information is used, for example, to look at the dietary targets on salt, fat and sugar. A fair amount of work is being done, but it is a very expensive area to survey. Given its responsibility for diet, FSS should look at whether the information that it gets back is fit for purpose or whether more could be done in that area.
On behalf of the committee, I thank you for the time that you have spent with us this morning and the evidence that you have provided.
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