Moved by Lord Kamall That the Grand Committee do consider the Food
and Feed Safety (Miscellaneous Amendments and Transitional
Provisions) Regulations 2022. The Parliamentary Under-Secretary of
State, Department of Health and Social Care (Lord Kamall) (Con) My
Lords, the Government’s priority is, as always, to ensure that the
high standard of food safety and consumer protection that we enjoy
in this country continues to be maintained now that the UK has
left...Request free trial
Moved by
That the Grand Committee do consider the Food and Feed Safety
(Miscellaneous Amendments and Transitional Provisions)
Regulations 2022.
The Parliamentary Under-Secretary of State, Department of Health
and Social Care () (Con)
My Lords, the Government’s priority is, as always, to ensure that
the high standard of food safety and consumer protection that we
enjoy in this country continues to be maintained now that the UK
has left the European Union. This instrument follows the 18 EU
exit instruments in the field of food and feed safety made during
2019 and 2020. It addresses two deficiencies identified in
retained EU law, and provides transitional arrangements for
labelling changes introduced as a result of EU exit. Since the
instrument is technical in nature, I hope noble Lords will allow
me to briefly summarise the changes we are making.
The instrument serves three key functions. First, it will ensure
that emergency powers can be applied equally to all food and feed
entering Great Britain. Retained EU Regulation 178/2002, on the
general principles of food law, provides Ministers with emergency
powers to suspend or restrict the placing of food or feed on the
market. This can be used where food or feed presents a threat to
human health. Legal analysis of Article 53 of that regulation
identified that, as worded, it is not possible for a Minister to
exercise those emergency powers on third-country food and feed
entering Great Britain via Northern Ireland. To correct this
operability issue, this proposed regulation includes a technical
amendment that will enable all Ministers to apply, equally, the
same emergency controls to all food and feed destined for our
market. The amendment does not extend the remit or gravity of the
controls that may be introduced, but will ensure that emergency
controls are exercisable equally across all parts of the UK.
Secondly, the statutory instrument ensures that authorising
provisions for feed additives and for GM food and feed
authorisations will be made by legislation. Legal analysis of
fixed and retained EU law identified that retained law on feed
additives and on GM food and feed contained certain omissions.
The regulations did not sufficiently make it clear that
Ministers’ authorisation decisions will be prescribed in
legislation. While this does not prevent Ministers from taking
decisions to authorise these products, provision for those
decisions to be implemented through legislation makes certain
their enforceability in law. It also ensures consistency with
other retained EU law in this area.
Thirdly and finally, the amendment provides a period of
adjustment for changes to labelling requirements made necessary
by EU exit legislation. In preparation for EU exit, changes were
made to the legislation on extraction solvents and quick-frozen
foods to reflect the fact that the UK would no longer be part of
the EU. As a result, relevant food placed on the market is
required to be labelled with the name and UK address of the legal
person responsible for it, rather than an EU contact and address.
This statutory instrument provides a period of adjustment in
those sectors, allowing for the continued use of existing labels
until 30 September 2022.
I should be clear that this instrument does not introduce any
changes that will impact the day-to-day operation of food
businesses, nor any new regulatory burden. The essence of the
legislation is unchanged. However, it provides benefit for
certain businesses by enabling a period of grace in the
introduction of labelling changes.
It is also important to note that we have engaged positively with
the devolved Administrations throughout the development of the
instrument. I take this opportunity to note that their ongoing
engagement has been warmly welcomed.
I reassure noble Lords that the overarching aim of this
regulation is to provide continuity for businesses and to ensure
that high standards of safety and quality for food and feed
regulation will continue across the UK. The changes do not affect
the essence of existing legislation. Having effective and
functional law in this area is key to ensuring the high standards
of food safety and consumer protection that we enjoy in this
country and to make sure that they are maintained in the
immediate and long term. I hope that noble Lords will feel able
to support the amendments proposed in this instrument to ensure
the continuation of effective food and feed safety and public
health controls.
5.30pm
The Deputy Chairman of Committees () (LD)
My Lords, the noble Baroness, Lady Brinton, is taking part
remotely. She is speaking as the Liberal Democrat Front-Bencher
but, as there are no Back-Benchers to speak, I invite her to
speak.
(LD) [V]
My Lords, I thank the Minister for his introduction to the Food
and Feed Safety (Miscellaneous Amendments and Transitional
Provisions) Regulations 2022, which propose three very differing
amendments to existing food safety measures. He was right to
start by saying that ensuring the highest levels of food safety
is absolutely vital.
The Joint Committee on Statutory Instruments has pointed out that
the second and third regulations come into force on the day after
the day on which these amendments are made, so once again they
breach the 21-day rule. It is such a shame that SIs and
regulations seem always to be dealt with as emergency items,
because this reduces the time available for Parliament to
effectively scrutinise legislation.
The first amendment is to Article 53 of the retained general food
law, to manage a problem that has arisen as a result of the
Northern Ireland protocol. I note that the Explanatory Memorandum
calls it a “deficiency”. It might perhaps be more honest to call
it a problem of the Northern Ireland protocol and the practical
effect it has had on border issues for those living in Northern
Ireland—how they have to juggle the tensions of a border in the
Irish Sea when third-party goods come into Great Britain via
Northern Ireland and where a serious risk to human health has
been identified with those goods.
It is right that the UK Government must correct regulations that
are not fit for purpose, and we note that these amendments to
Article 53 do not change the purpose or function of the original
provision but there is now full protection for such emergency
measures, regardless of where the goods have come from.
The second amendment relates to the authorisation of provisions
for feed additives and for GM food and feed, which will now be
through legislation, bringing them into line with other retained
EU food and feed law. That is particularly welcome. There is a
lot of suspicion about GM food and feed, and it is important that
there is a vehicle through which it can be scrutinised carefully.
Parliament is the right place for that to take place.
The third and final change is a sensible step to ensure that
businesses have a slightly longer period to move from EU to UK
labelling requirements, until 30 September this year. For some
time, food businesses have been asking for a longer period, as
well as for labelling requirements to be as close as possible to
the EU requirements. The latter is not covered by this SI, but I
hope that the Minister will continue to listen to UK food
businesses which want to continue to sell into the EU and which
must also abide by the EU labelling requirements. I thank the
Government for the extension to the period during which the EU
ones can be used.
The SI brings us back to the wider issues of the Northern Ireland
protocol. That is obviously not on the agenda for today, but I
want to say that, from these Benches, we always warned that there
would be problems for goods travelling into Great Britain via
Northern Ireland and for businesses there, which continue to
express real concerns about the UK’s decisions and legislation
between 2018 and 2020. Whether one agrees with them or not, it is
good that these three corrections and amendments will at least
sort out some of those minor problems.
(Lab)
My Lords, I am grateful to the Minister for setting out the
rationale behind this eminently sensible statutory instrument,
which deals with a number of significant technical issues
relating to the Food Standards Agency, some of which have come
about because of the Northern Ireland protocol. They need to be
resolved, and from these Benches we are of course happy to
support this statutory instrument.
I add that the Explanatory Memorandum is very helpful in
outlining the approach that the FSA is taking. I will just pick
up on a few points. First, paragraph 7.7 refers to
“An analysis of the emergency powers for”
food and feed control, which revealed that these powers could not
be deployed as effectively as required. I am interested in
exploring the context. It would be helpful if the Minister could
advise on whether this analysis was through a hypothetical
desk-based exercise, or whether the situations referred to
actually occurred. For example, did goods identified as
presenting a serious threat to human health enter Great Britain
through Northern Ireland or did that not happen in reality?
I welcome the clarification that the GM and feed additive
authorisations will be dealt with through an SI. It would be
helpful if the Minister could confirm whether this will be
through the negative or affirmative approach. Also, are there any
implications for the Government’s longer-term strategy for GM
products, given the recent statutory instrument that changed some
of the rules on research and gene-edited crops?
On the issue of labelling, it would also be helpful if the
Minister could comment a bit on whether he feels that the date in
place is the right one. I say that because the food production
sector finds itself under pressure, of course, and we want to
ensure that this is a practical step.
Throughout the consultation, the National Farmers’ Union has
sought clarification on the UK’s relationship with the European
Food Safety Authority. The NFU has stressed the importance of the
UK’s close collaboration with the EFSA on equal terms. Can the
Minister comment on the Government’s intentions for their
relationship with the EFSA in the context of this statutory
instrument, given its importance to our food industry? I would be
most grateful.
I have a final point to raise. With regard to the consultations,
one observation by the sector was about the expectation that
these changes to the regulations could be read through in under
an hour, such that businesses, regulatory agencies and councils
would be able to work out in that short period how to apply the
changes to their organisations. I know that this was regarded as
somewhat overoptimistic, but has any further thought been given
to an assessment of just how easy it will be to work with these
regulations? With those comments, I offer our support for these
regulations and thank the Minister in advance for the reply that
I know he will give.
(Con)
My Lords, I thank both noble Baronesses for their contributions
and for their general positive response. Once again, I can only
apologise for the fact that that some provisions are late. That
is an issue that I constantly raise internally and I understand
the criticisms.
I will try to address as many of the questions asked by the noble
Baronesses as I can before I conclude. On the Northern Ireland
protocol, one thing we are looking at is the United Kingdom
Internal Market Act and its purpose of promoting the functioning
of the internal market, given that we have the Northern Ireland
protocol. The Act specifically serves to strengthen and maintain
Northern Ireland’s position in the UK internal market. In terms
of the bigger picture and how the Northern Ireland protocol works
in future, we are hoping that will be done via the UK internal
market Act, taking account of that protocol.
The SI makes provision for a specific transitional period to
allow the industry to use up existing labelling stocks. A period
of 12 to 24 months is indicated as being sufficient time to use
up labelling stocks; some quick-frozen produce can also have a
shelf life of up to two years. However, if there are still
concerns from industry, no doubt we will look at them. We are in
constant conversation with industry and a whole range of sectors
related to health and other issues.
I hope that covers some of the questions that the noble Baroness,
Lady Brinton, asked. Once again, if I have not answered all the
questions, we will check Hansard and make sure that we sweep up
any answers to both noble Baronesses.
The noble Baroness, Lady Merron, asked how the issue was
identified. It is hypothetical; nothing has happened, there was
no breach of standards. The procedure will be a negative
procedure for authorisations. We have had the first group of
applications for authorisations, which have progressed through
the risk analysis process, and advice has been prepared for
Ministers. This amendment is required to empower Ministers to
prescribe the authorisation by regulation.
The wider question of the future of GM and gene editing is not
considered by this SI, and really it is a matter for the
Secretary of State for Environment, Food and Rural Affairs. Of
course, if the noble Baronesses want more information, I am very
happy to contact that department. For now, the commercial
cultivation of gene-edited plants and any food products derived
from them will still need to be authorised in accordance with
existing GMO rules.
The UK has developed an enhanced risk analysis process, through
the FSA, and we will seek close co-ordination with the EFSA. It
does not mean we will always align, but it is really important to
make sure that we have a strong relationship. Quite often,
clearly, the issue of food safety is something that is shared by
a number of jurisdictions, not just the UK and the EU, but in
fact globally. So we will be looking at that.
In closing, I am grateful for the noble Baronesses’ contributions
today. As I have said, if I have not answered questions, I hope,
after a quick read of Hansard, I will try to sweep them up. I
grateful to the noble Baronesses for their support. We want to
make sure that there is a smooth transition for certain
businesses in adjusting to the new labelling requirements. I take
on board the comments made and I beg to move.
Motion agreed.
|