I thank all noble Lords who have contributed and congratulate the noble Lord, Lord Hunt, on securing this debate. It is an important subject and it is right that we take time to consider it. I know
that he takes a keen interest in NICE’s work from his previous role as the first Minister with responsibility for NICE, and it is a privilege to have taken on his mantle some years later.
This year marks a significant milestone for NICE, as it celebrates its 20th anniversary, during which time it has transformed the way in which decisions are made in the health and care system. I echo the comments made by the noble Baroness, Lady Thornton, who referred to NICE as a jewel in the crown of the UK life sciences ecosystem. She is absolutely right that we must ensure that we not only protect it but promote its success. Since its inception, NICE has played a vital role, not only in securing maximum value from health spending but in ensuring that patients are able to benefit from rapid access to effective new drugs and other treatments. The noble Lord, Lord Hunt, hit the nail on the head when he said that that balancing act in the health system is so challenging.
Of course, the NHS is required to fund the treatments recommended through NICE’s technology appraisals and HST evaluation programmes, so that they can be provided if a patient’s doctor says that they are clinically appropriate for the patient. Over the past 20 years, more than 80% of NICE’s recommendations have supported use of the technology assessed, meaning that many thousands of patients have benefited from rapid access to effective new treatments. A less-frequently reported statistic is that 75% of HST applications have also gone through, which is encouraging.
Recent IQVIA research has just been published which showed that, despite some of the frustrations we have with update and access—which is something we are working hard on—the UK is in fact one of the fastest countries in Europe to get products through its regulatory system. We can be very proud of that, and must protect it.
I know that your Lordships will agree not only that it is extremely important that we have a system such as NICE in place to ensure the NHS spends its money in the most effective way possible, but also that it is critical that NICE operates on a sustainable footing so that it continues to be responsive to developments in the life sciences sector, to which noble Lords all referred.
To date, as has been mentioned, NICE’s TA and HST programmes have been funded through government resources but, as is common with government bodies, it is right that NICE considers how to operate to the utmost efficiency, and that those who stand to benefit from services contribute.
This is standard procedure and a standard model for many organisations and ALBs such as NICE. It is standard for the MHRA, the HTA, the CQC and for HTAs in other countries, so we are not operating an unusual procedure here, as the noble Lord, Lord Hunt, mentioned. I was grateful for his support for the charging model.
However, recognising the need for sustainability must be balanced with the imperative to encourage innovation, and the Government and NICE believe that the most appropriate and sustainable model for NICE’s TA programmes in future is for it to levy a proportionate charge on companies that benefit directly from its recommendations. This goes right back to a
recommendation of the triennial review of NICE in 2015, so long-term work has been going on in this area. Recognising the importance of getting it right, the Government consulted on the draft regulations. That consultation has been referred to by noble Lords. At that point, as part of those proposals, the Government proposed the 25% discount for small companies. The consultation also sought views on a proposal to enable NICE to recruit appeal panel members engaged in the provision of healthcare in the health services across the UK instead of just England. This has not been mentioned and I know is widely supported, but I just wanted to point out that fact, which we are very pleased about.
As was raised by the noble Baronesses, Lady Thornton and Lady Jolly, there were 78 responses to the consultation, around half of which represented views from the life sciences industry, including pharma companies, industry representatives, consultancies and medtech companies. Other responses came from patient groups, NHS organisations and individuals. Although, as has been said, the majority of respondents—62%—disagreed with the specifics of the proposal to charge companies for making recommendations, the analysis showed that just over half of respondents agreed that life sciences companies should contribute to the cost of developing NICE recommendations, which is why further work was done to develop the charging proposal but refine it.
Respondents also supported, by 59%, a mechanism for reducing the impact on small companies, but felt that the proposed 25% discount did not go far enough. Other more specific concerns were raised about the potential impact on patient access to new treatments, in particular for rare diseases, the impact on NICE’s independence, and the analysis contained in the impact assessment.
The SLSC also picked up on issues in its report, and I will address some of those in response to points raised by the noble Baronesses, Lady Thornton and Lady Jolly. The Government considered the issues raised in the consultation very carefully and carried out further analysis to feed into the final impact assessment. We concluded that it was appropriate to make two main changes to the policy in light of the consultation responses. These particularly dealt with concerns about the design of the charging with respect to SMEs. I know that noble Lords are well aware of those concerns.
There is an increased discount for small companies of 75%, to minimise barriers to the participation of small companies wishing to bring forward new products. I realise that many feel that that did not go far enough but, to address that concern, it also included the new power to enable the Secretary of State to direct NICE in specific cases to calculate charges on what it considers to be the appropriate commercial basis. This provides more flexibility for amending charges, should that be required in future, subject to consultation with stakeholders. For example, we may see different types of innovation, including devices or digital products going through TA programmes, and this provides flexibility for the Secretary of State to direct NICE to
propose charges at a level appropriate to those markets. I think that responds to the point raised by the noble Lord, Lord Hunt.
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As I mentioned earlier, I should like to go through a couple of points raised by the SLSC in its report. The committee, and the noble Baroness, Lady Thornton, noted the potential for conflicts of interest as a result of companies paying for NICE recommendations. We need to give due credit to NICE’s world-leading reputation. It was founded on independence and transparency in the work it carries out. The charging model introduced includes clear safeguards to ensure that this remains unchanged. For example, with the exception of small companies, companies will be required to pay the full cost up front, regardless of the outcome, and no one directly responsible for making NICE’s decisions will stand to benefit from the income that NICE receives from companies. NICE’s recommendations and decisions on the most appropriate programme—TA or HST appraisal—for individual products are also made transparently and in accordance with its published methods and processes.
Secondly, the committee raised the question of the impact on availability of drugs for rare diseases, as did the noble Lord, Lord Hunt. The Government considered whether products for rare diseases should benefit from a discount in common with small companies, but did not consider this necessary at this point, because companies already benefit from a significant set of incentives to develop drugs for rare diseases, and worldwide orphan drug sales are forecast to grow at 11.3% per year from 2018 to 2024, double the rate forecast for the non-orphan drug market. The noble Lord, Lord Hunt, was right to point out that we are also requesting that NICE review its TA and HST methods, specifically to address challenges to cohorts and data management as we committed to within the voluntary scheme. I have asked Andrew Dillon to ensure that the review takes into account the benefits offered by new treatments for severe life-threatening and rare diseases, so this area will not go untested.
Thirdly, the impact on the attractiveness of the UK as a country to invest in and launch new drugs, particularly at the same time as Brexit, was raised by the noble Baroness, Lady Jolly. It is important to note that the cost to companies of a NICE assessment will represent a very small percentage of the potential revenues that a company will generate from an effective new treatment, but we have still said that we will keep the impact of those costs under review in the context of the wider impact on companies of Brexit. We have made that commitment.
The Government’s overall aim remains that patients in the UK continue to access the best and most innovative medicines and devices and are assured that their safety is protected through ongoing co-operation and the strongest regulatory framework. Your Lordships will understand that our key guiding principles are to ensure that patients are not disadvantaged, that the UK will continue to play a leading role in promoting and ensuring public health, and that the industry must be able to get its products into the UK market as quickly and simply as possible.
Lastly, the noble Baroness, Lady Jolly, also raised the point that the committee queried how the savings generated from the introduction of charges will be used. As a public body, NICE will continue to be accountable to Parliament for how it uses the government money allocated to it, and I assure your Lordships that that will remain unchanged by the introduction of charging.
I close by stressing that the Government share the view that we have heard today about the vital importance of NICE’s work. These matters are very important to all of us. With the changes we have made in response to the consultation comments, I am confident that the introduction of charges and the charging regime for NICE recommendations will enable it to continue to be sustainable and develop its recommendations with the same authority, transparency and impartiality that have been the backbone of its world-leading reputation, and that the UK life sciences sector will remain as strong as it has ever been, if not stronger.