Last updated on 06 Aug 2021
HTA Strategy 2020-23
Introduction from the HTA’s Chair
I am pleased to introduce the Human Tissue Authority’s Strategy for the period 2020-23.
Since taking up the role as the HTA’s Chair in November 2019, our operating environment has fundamentally changed as the UK responds to the COVID-19 pandemic. It has been a challenging time for everyone and, like others, we shall have a great deal to learn from the experience of regulating remotely and maintaining our focus on risk based and proportionate regulation. We are pleased to have played our part in ensuring the public can continue to have confidence that patient safety is at the heart of what we do.
Although this is a period of significant change and uncertainty, the HTA’s role remains vital. Our guiding principles, values and strategic aims are central to what we aim to achieve.
Our Strategy continues to focus on the three key themes of sustainability, resilience, and agility.
In the period covered by this Strategy, we will continue to:
- license and inspect establishments, in order to monitor compliance with legislation and best practice and take action where it is required. We will do this in an agile way, recognising that ways of working have changed and that different risks will have emerged;
- provide advice and guidance to the public and professionals with an interest in the areas we work in and involve them in our work where appropriate;
- work closely with our key partners across the system in order to ensure a consistent and joined up approach to healthcare regulation nationally;
- ensure that we maintain public confidence in the systems we regulate, through an open and transparent approach to reporting and acting in an effective manner on any serious failures uncovered or concerns held.
To support this, we will continue with our programme of improvement examining how we can most effectively deliver our services in the future. This work will address, amongst other things, how we can better ensure that we: use our intelligence and knowledge of risk to support our inspection programme and inform our proportionate regulatory approach; engage with and involve the public and professionals through as wide variety of channels as possible and seek out new and useful ways to build and strengthen relationships with others.
The UK is extraordinarily well placed to play a leading role in the growth of the life sciences sector, with strengths in innovation, research, healthcare and business.
The HTA is not alone in the regulatory environment in wanting to make the UK a great place for research and innovation to thrive, whilst ensuring patient safety is not compromised.
We anticipate that the next few years will be a challenging period, but with this challenge will come opportunities. As a regulator of six diverse sectors, we will play our part in building an effective regulatory environment that supports innovative, emerging technology and that can adapt to new and emerging risks.
I look forward to working with you to achieve these goals.
About the HTA
The HTA is an executive Non-Departmental Public Body sponsored by the Department of Health and Social Care, established under the Human Tissue Act 2004.
Our overall goal is to maintain public confidence by ensuring that the removal, storage and use of human tissue and organs are undertaken safely and ethically, and with proper consent, in accordance with the provisions of the Human Tissue Act 2004, Human Tissue (Quality and Safety for Human Application) Regulations 2007 (as amended) and the Quality and Safety of Organs Intended for Transplantation Regulations 2012 (as amended).
We also have a role in maintaining both public and professional confidence, by assuring that human material being used by professionals has been obtained with the proper consent and is managed with appropriate care.
- We license organisations that remove, store and use human tissue for activities set out within the Human Tissue Act 2004.
- We license organisations involved in preparing tissues and cells for use in patient treatment as required by the Human Tissue (Quality and Safety for Human Application) Regulations 2007.
- We license organisations involved in organ donation and transplantation as required by the Quality and Safety of Organs Intended for Transplantation Regulations 2012.
- We monitor and inspect or audit organisations to ensure they comply with the requirements of the legislation and our Codes of Practice.
- We use our powers to take regulatory action where we identify non-compliance.
- We assess living organ donations to ensure donors are protected from duress or coercion, and that no reward is offered or given.
- We provide information, advice and guidance to the public and professionals about the nature and purpose of activities within our remit.
- We monitor developments relating to activities within our remit and advise Government on related issues.
In addition to our statutory role we are increasingly called upon to provide advice on areas related to, but not specified in, our legislation. This is particularly important in areas of emerging technology and cutting-edge research not originally envisaged when the Human Tissue Act was enacted.
Areas which we regulate
Removal, storage and use of human tissue and organs for a number of activities and scheduled purposes as set out in the Human Tissue Act 2004: post-mortem examination, anatomical examination, research, transplantation and public display.
Procurement, testing, preservation, processing, storage, distribution, import and export of tissues and cells for use in patient treatment (human application).
Donation, testing, characterisation, procurement, preservation, transport, transplantation and disposal of organs for transplantation.
Our remit under the Human Tissue Act 2004 extends to England, Wales and Northern Ireland; however, we also carry out some activities in relation to the approval of living organ donations on behalf of the Scottish Government. Our remit as the Competent Authority for the quality and safety of tissues, cells and organs used in transplantation extends to the whole of the UK.
We license over 800 premises across the six sectors that we regulate and publish standards and requirements that those working within these regulated fields must meet.
Whilst the HTA has a statutory duty to superintend compliance and an influential role in promoting good practice, public confidence in the use of human tissue cannot be safeguarded by the HTA alone. Public confidence is also dependent on the individuals and organisations that undertake activities within the HTA’s regulatory remit acting within the standards and requirements of the legislation.
Four guiding principles continue to drive our work and underpin our regulatory framework. They should be followed in dealing with human bodies, tissue and organs:
- Consent - and the wishes of the donor (or in some cases, their nominated representatives or relatives) are the primary consideration when removing, storing and using human tissue
- Dignity - is paramount in the treatment of human bodies and tissue
- Quality - must underpin the management of human bodies and tissue
- Honesty and openness - are the foundation of communications in matters pertaining to the use of human tissue and bodies
Our values as an organisation in carrying out our role, expressed in all interactions are:
- Professionalism - the high standards we apply in the conduct of our individual and collective responsibilities
- Respect - proper regards for the abilities and perspectives of others
- Expertise - the skills, knowledge and experience we apply for the benefit of our stakeholders and each other
- Agility- rapid and positive response to changes in the internal and external environment without losing momentum
We group our key activities into three themes:
- Delivery - how we achieve our strategic objectives today
- Development - how we will improve in the future
- Deployment - how we effectively use our people and resources
- Through these themes, our strategy sets out the ways in which we will strive to be a more resilient, sustainable and agile organisation. in order to meet the challenges ahead.
We are now in the third year of a multi-year strategy stemming from a review that took place in 2017. At this time, the HTA undertook a fundamental evaluation of the extent to which our strategic approach protects public and professional confidence in the proper use, and quality and safety of, human tissues, cells and organs. We based this evaluation on evidence and analysis from a variety of sources, including the views of those working in establishments we regulate, an evaluation of public opinion, analysis of the data we hold, and the views and opinions of HTA staff and Authority Members.
An assessment of the evidence provided us with great reassurance that both the public and professionals think we are on the right track with our regulatory approach. However, the review identified opportunities and challenges relating to our operating environment that require us to adapt as an organisation.
As a statutory body, our aim remains unchanged. As such, our review focused on evaluating our future operating environment and whether our resources are optimally aligned to where the risks are greatest.
Our organisational change programme in 2020/21 is focused on development of our systems and processes to support our ambition of being a data and intelligence-led organisation that is able to adapt to keep pace with a changing operating environment.
The pace of innovation in cell, tissue and organ-based therapies, in life sciences research, and the use of digital imaging and artificial intelligence in pathology, all have the potential to impact hugely on the way the sectors we regulate work. Many of these developments were unforeseen when the legislation was framed, and we need to be realistic about the limited opportunity for legislative change.
As one of the regulators operating in the field of life sciences, we are clear that effective regulation can make a positive contribution to patient outcomes and economic growth. We are determined to play our role in the ambitious plans set out by the Government through the Industrial Strategy. In the last two years we have been fully engaged in preparations for the UK’s exit from the European Union and a contributed to the development of legislative changes to consent provisions for organ donation in England through extensive stakeholder engagement and preparation of a Code of Practice bringing the legislation into effect.
We recognise that our staff are our key asset – their skill and dedication lie at the heart of our organisation - and therefore staff recruitment and retention contribute significantly to our strategic risk. As the regulator of six increasingly complex and diverse sectors, and with a continued need to control our resources, we are acutely aware of the demands this can place on our staff.
Our strategy, therefore, continues to focus on the steps we need to take in order to operate in a more sustainable way, building in greater resilience and agility in the face of increasing complexity and uncertainty in our external environment.
By sustainability, we mean taking a new approach to recruiting, developing and retaining high quality staff and working in new ways to reduce the growing pressures on the staff we have.
By resilience, we mean adapting our operating model to retain staff for longer, and developing strategic alliances with other organisations to put us in a better position to manage unexpected demands.
By agility, we mean providing a highly responsive regulatory framework that supports innovative uses of organs, tissues and cells, burnishes our reputation as an expert regulator and actively supports the Industrial Strategy for Life Sciences.
Success will mean retaining alignment with core principles and values, whilst developing our staff in a flexible manner to lead and adapt to innovations in our area of regulation.
In order to meet the challenges ahead we require continued focus on our:
- People - recognising our staff as our key asset, widening the pool of candidates for recruitment beyond the South East and investing in training and development
- Business Technology - ensuring our systems are not reliant on location and making strategic choices about key business systems
- Information and data - meeting our obligations relating to data security and using information and data as a key strategic resource
- Finance - being clear about managing our fee levels based on workload and regulatory effort, including longer term planning to ensure continued financial viability.
Our strategic approach
Our strategic approach is based on being clear on the risks we are regulating, being proportionate and targeted in regulating those risks, taking into account the role of professional bodies and other regulators, and using the minimum necessary direct intervention to achieve compliance and improvement.
Effective communication is also integral to our strategic approach to ensure that professionals can access advice and guidance from us, and that the public is clear on what they should expect from us and the areas we regulate. How we do this in our daily operation is described in the Delivery section of this strategy.
The HTA has never been an organisation to stand still, and is continually striving to enhance public confidence, better target our regulation, and adapt as an organisation. The Development section of the strategy describes the renewed focus for our development goals during this strategic period to ensure sustainability, resilience and agility in addition to continuing our programme of continuous improvement.
Neither Delivery nor Development is possible without resources. The Deployment section of the strategy describes how we lead, manage and develop the HTA’s people, how we raise and use our finances and our plans for accommodation and other key assets.
Our objectives are therefore grouped into three themes. All of these aspects will require a careful balance to make the most of our limited resources and ensure success in delivering our overall aim.
- Delivery - to deliver the right mix of operational activity to maintain public and professional confidence.
- Development - to make the right investment to continuously improve delivery and deployment.
- Deployment - to make the most effective use of people and resources in pursuit of our goals.
Our regulatory approach aims to be in line with the principles of better regulation and the Regulators’ Code. This means that we primarily focus our regulation and resources on areas that involve an inherently greater risk to patient safety and public confidence if standards are not maintained.
We employ a range of regulatory tools in order to ensure compliance with the legislative requirements, including licensing, inspection, reporting requirements and the provision of advice and guidance.
The legislation prescribes certain activities that can only be undertaken by a licensed establishment.
We license establishments across six sectors:
- Post Mortem, Public Display, Research, and Anatomy (under the Human Tissue Act 2004)
- Human application – tissues and cells used in patient treatment (under the Human Tissue (Quality and Safety for Human Application) Regulations 2007)
- Organ Donation and Transplantation (under the Quality and Safety of Organs Intended for Transplantation Regulations 2012)
The establishments we license must adhere to our standards, which align to our core principles. We welcome the significant degree of trust that the vast majority of our licensed establishments have in us, as demonstrated by their openness and willingness to improve. As a result, we only use significant regulatory action when it is appropriate and in the public interest.
Inspections or audits
We conduct site visits of licensed establishments in order to assess whether our standards are being maintained. We schedule inspections based on a number of factors, including the legislative requirements, and according to the risk of the activities being carried out. We also undertake non-routine inspections, both announced and unannounced when we have information which indicates that an inspection may be necessary due to the risks presented.
In response to the COVID-19 pandemic, we are adapting our oversight model to develop a remote form of assessment. We will build on and modify this model over the coming months as we continue to target our resource to areas where risk is greatest, with a view to ongoing use within our overall regulatory framework.
We require incidents and events which pose the highest risk to public confidence and patient safety to be reported to us by licensed establishments. This reporting, along with issues and complaints about licensed establishments that are raised with us by third parties, allows us to take action if required.
Living donation assessment
The HTA maintains a system to ensure that donations of organs or tissue for transplantation from living people are given without coercion or reward. The system relies on donor and recipient interviews, undertaken by a group of independent and accredited assessors. They are predominantly volunteers whom we train, accredit and support in order to fulfil our statutory functions. Complex cases are reviewed by panels, made up of HTA Board Members.
Advice and guidance
We provide advice and guidance to both the public and professionals and recognise the value in supporting establishments to comply, rather than dealing solely with non-compliance. We publish Codes of Practice and sector specific advice and guidance, as well as answering individual enquiries from establishments and members of the public.
Communication and engagement
We recognise communication as a key component of effective regulatory delivery. We utilise a range of channels to communicate with professionals, the public and key stakeholders to ensure that there is confidence in HTA regulation and in the services being regulated. We share learning gained through our newsletters and publications and aim to use our regulatory insight to provide guidance that promotes compliance and provides clarity for our stakeholders on how to meet our regulatory expectations. We engage through stakeholder groups to ensure we make decisions that take into account, as far as possible, the operational realities faced by professionals and the concerns of the public.
Our formal groups, which report to the HTA’s Board include:
- Stakeholder and Fees Group
- Histopathology Working Group
- Transplantation Advisory Group
We also engage virtually via our public panel and licensed establishment engagement programme, which provide fora for wider participation and further opportunities for those interested or affected by our work to be involved in, and inform it.
Stakeholder feedback is crucial to understanding the effectiveness of our regulation and identifying opportunities to adapt or expand on our regulatory approach. During this strategic period, we will use results from a recent stakeholder evaluation exercise to make sure that our regulatory approach and engagement strategies remain fit for purpose and reflect, where possible, the views and experience of our regulated establishments.
Working with other organisations
Many of the establishments within our remit are also regulated or accredited by other bodies. We continue to see collaboration as a key tool for achieving benefits for professionals and the public that produces joined up results, reduce our costs or reduces regulatory burdens. The HTA has bilateral agreements with organisations across the areas we regulate. We will look to build on these through opportunities to strengthen both formal and informal working arrangements
- Deliver a risk-based, data-driven and proportionate programme of licensing, inspection and incident reporting, targeting our resources where there is most risk to public confidence and patient safety.
- Deliver effective regulation of living donation.
- Provide high-quality advice and guidance in a timely way to support professionals, Government and the public in matters within our remit.
- Be consistent and transparent in our decision-making and regulatory action, supporting those licence holders who are committed to achieving high quality and dealing firmly and fairly with those who do not comply with our standards.
- Inform and involve people with a professional or personal interest in the areas we regulate in matters that are important to them and influence them in matters that are important to us.
- Maintain our strategic relationships with other regulators operating in the health sector.
In the period covered by this strategy, we will:
- Ensure that new applications meet appropriate standards before issuing a licence.
- Further utilise our knowledge of risk in each sector to apply the right mix of regulatory tools to support compliance.
- Undertake a risk-based programme of inspection which provide assurance that standards are being maintained.
- Publish exception-based reports of inspections in the interests of transparency and to share learning.
- Take a proportionate and risk-based approach to non-compliance, and ensure that where there are shortfalls against standards, these are rectified within agreed timescales or escalated appropriately.
- Ensure decisions on living organ donation cases meet agreed service standards in a way that provides the necessary protections.
- Engage with, and involve, public and professional stakeholders in our work using a wide variety of channels.
- Use the results of our public evaluation to create awareness of what drives public confidence, what the public are most interested in, and why.
- Seek out opportunities to build new collaborations for the benefit of stakeholders.
To ensure that the HTA’s regulatory approach remains relevant, we actively prepare for the future. We do this through our development activities. As outlined in the Strategic Review section, in this three-year period our development goals will focus on building resilience, agility and overall sustainability through a programme of more significant organisational change activity, alongside a plan of continuous improvement.
We see innovation across all the sectors we regulate and actively horizon scan to keep abreast of developments to inform our work, often in collaboration with other organisations. The pace of change requires a highly responsive regulatory framework that supports innovative uses of organs, tissues and cells.
Where emerging issues can be accommodated within the current regulatory framework, we will work to achieve this with agility, proportionality and appropriate assessment of risk. Where they cannot, we will advise relevant government, professional and public stakeholders, and actively consider the use of alternative approaches where this is appropriate to risk.
In the Human Application sector, we will continue to work closely with the Medicines and Healthcare products Regulatory Agency and other regulatory bodies on the Regulatory Advice Service for Regenerative Medicine (RASRM) which we see as a key foundation for the future regulation of novel tissue and cell therapy-based products. As well as helping the sector to navigate the regulatory landscape, this joint working is essential to our ability to remain agile and to regulate effectively in a changing environment.
In living organ donation, wider use of the UK living kidney sharing scheme continues to place pressure on staff resource. We have made good progress in improving the resilience of our Independent Assessor system and we will continue to examine the way in which we as the Authority undertake approvals.
The Organ Donation (Deemed Consent) Act 2019 came into force in England on 20 May 2020, changing the legal basis for consent for deceased organ donation in England. We have worked closely with the sector to revise our Codes of Practice to reflect the changes in legislation. Close engagement with public and professional stakeholders will remain a key priority as the changes come into effect.
Following the UK’s exit from the EU, we are continuing to work closely with the Department of Health and Social Care to ensure preparations are in place throughout the transition period and assess any implications for our regulated sectors.
Although in general, we see a high level of compliance in licensed establishments, we are continuing to see an increase in the number of shortfalls against standards on inspection in some sectors and have identified areas where we could strengthen our oversight. We will use the data and insight that we hold, and close links with key stakeholders, to implement a targeted approach aimed at addressing these issues.
Better use of data and information
We already use data and information to inform our risk-based approach to regulation and have implemented measures to more routinely review and utilise core data. We recognise that we can further improve the quality, and make better use of automation and technology to manage the data and information we hold, in order to ensure we identify trends and prioritise and target resources effectively across the organisation.
In addition to seeking continuous improvements to processes, this strategic period will see us invest significant resources in developing our people, business technology and estates planning. Balancing how we use our resources between strategic development, continuous improvement, and core delivery activities will mean a greater emphasis on clarifying priorities, and promoting cohesive, organisation-wide approaches to addressing key business concerns.
As an organisation, we have responded effectively to the recent move to remote working, minimising the impact of the changes on our staff and their ability to deliver our regulatory functions. We will continue to build on the work we have already done and any learning we can use from this as we move to new ways of working in the future.
Further details on how we will shape our future approach are described in the deployment section of this strategy.
We will reflect our experience of regulating across diverse sectors in submissions and dialogue on the future of regulation, particularly in the context of the Government’s Industrial Strategy and EU Exit, and in sharing our experiences of adapting in response to the COVID-19 pandemic. We will be available to offer advice and guidance to colleagues across government and those we regulate as and when it is needed and work in partnership with innovators to advise, guide and shape best practices to drive consistent implementation.
Our development objectives are:
- Use data and information to provide real-time analysis, giving us a more responsive, sharper focus for our regulatory work and allowing us to target resources effectively.
- Make continuous improvements to systems and processes to minimise waste or duplicated effort, or address areas of risk.
- Provide an agile response to innovation and change in the sectors we regulate, making it clear how to comply with new and existing regulatory requirements.
- Implement and embed a future operating model, which builds our agility, resilience and sustainability as an organisation.
In the period covered by this strategy, we will:
- Further plan, develop, and implement an organisational change programme.
- Prioritise engagement with stakeholders to support the implementation of deemed consent in England.
- Continue to develop the use of our data and intelligence functions in the management of risk.
- Continue to work with central Government and our licensed establishments to support cross-organisational work on the UK’s future relationships with the EU and the rest of the world.
- Continue to develop approaches to engaging with Designated Individuals and licensed establishments as a key tool in ensuring compliance.
- Develop tools to improve how we prioritise and plan regulatory activities and manage resources, including more effective use of information and data.
- Continue to upgrade and develop core business systems, website, and online portal to better meet business needs and the needs of stakeholders.
- Continue to use our unique position to advise the Government in matters relating to our remit.
Our staff are our key asset and are fundamental to successful delivery of our objectives. Our staff survey gives us great reassurance that the HTA is a good place to work, but also offers insight into areas we can improve. Over the last three years we have made great progress on updating our people strategy, in order to achieve our vision of a more resilient and sustainable organisation.
As we begin to benefit from recruiting staff from a wider geographic pool, we will continue to build on the work we have done to remodel induction and training. This will allow staff to become competent more quickly and means that we will be less dependent on the location of our staff.
As a small, expert regulator, it is imperative that we retain the specialist skills of staff for longer, and that we improve the resilience of standalone roles. We will continue to promote work/life balance and flexible working, with a renewed focus on effective line management, training and development to make the best use of expert resources.
Our People Strategy, as outlined above will largely drive our approach to estates. As an organisation that works remotely by design, we will continue to focus our efforts on ensuring that our culture and connectivity are maintained. We will continue to control accommodation costs as far as possible by sharing office space and through improving the ways in which we use the space that is available to us.
During this strategic period, we will move our office base to Stratford, along with other healthcare regulators. Through co-location, we will make the most of any opportunities for combined ways of working.
Our business technology has never been more crucial to the success of the organisation and underpins much of what we set out to achieve. Our strategic vision requires development of IT architecture, which is not dependent on location. We will support our staff with the technology they need to work effectively and efficiently, in the office and remotely. We also recognise the opportunities for technology, digital and data to improve the services we offer, reduce burden, and target our resources most effectively.
We take our commitment to information and cyber security very seriously and will strive to meet our obligations under data protection legislation, the National Data Guardian’s data security standards and relevant UK Government cyber security frameworks.
The HTA is funded through licence fees and Grant-in-Aid from the Department of Health and Social Care. For a number of years, we have worked hard to keep costs down by finding efficiencies, sharing office space and sharing Director and Head posts with the Human Fertilisation and Embryology Authority (HFEA). Our recent review of the arrangements with HFEA highlighted further opportunities to boost the resilience of both organisations by developing a stronger strategic alliance.
We are aware of the budget constraints faced by many of our licensed establishments and remain committed to living within our means. As part of our sustainability programme, we aim to signal our budget intentions over the next three years, with a view to providing certainty on fee levels for establishments. In this strategic period, we will ensure that our regulatory model ensures that our fee level is kept in line with our regulatory approach. Robust oversight and governance of our organisational change programme will ensure that we use our funds prudently to achieve tangible benefits for our stakeholders.
Our Deployment objectives are to:
- Manage and develop our people in line with the HTA’s People Strategy.
- Ensure the continued financial viability of the HTA while charging fair and transparent licence fees and providing value for money.
- Provide a suitable working environment and effective business technology, with due regard for data protection and information security.
- Plan and prioritise our resources to carefully balance activity across the organisation.
In the period covered by this strategy, we will:
- Act on the feedback provided by our staff to address key issues of concern.
- Build on the remodelling of our training and induction programme.
- Identify and strengthen the capabilities we will need to achieve success over this strategic period.
- Develop more formal arrangements for greater use of home working to support our recruitment strategy.
- Give greater priority to information management and risk, ensuring that we comply with our requirements under relevant Data Protection legislation.
- Implement the recommendations of the shared services review with HFEA and continue with measures to improve the resilience of both organisations.
- Improve our video conferencing, online meeting, and collaboration capabilities.
- Produce an options appraisal for different models of working as an organisation, which puts our staff at the heart of what we do.
- Relocate to a Government Hub in Stratford.
The HTA’s Board is made up of a Chair and twelve Members:
- Ten are appointed by the Secretary of State for Health and Social Care;
- One is appointed by the Welsh Cabinet Secretary for Health and Social Services; and
- One is appointed by the Minister of Health in Northern Ireland.
The Board is made up of both lay and professional Members and currently includes an organ donor and a transplant recipient. The professional Members of our board come from medical and scientific backgrounds linked to our work, and the lay Members bring a wide range of business, commercial, academic, and public sector experience.
The Board’s primary role is to ensure that the HTA’s statutory responsibilities are met and discharged effectively. It achieves this by setting the HTA’s strategic direction and providing both support and challenge to an Executive, which is responsible for the delivery of these responsibilities on a day-to-day basis.
While the Executive implements this strategy by way of business plans, there are mechanisms in place by which the Board steers, scrutinises and reviews performance.
The HTA holds four board meetings per year, one of which is in public, and an annual strategy away day. These meetings provide the opportunity to assess a range of management information and more detailed reports on progress against elements of the strategy. They also allow the Board to hold the Executive to account for the HTA’s performance.
Standing items reported to the Authority include:
- Chief Executive’s report – to provide an overall assessment of the HTA’s performance and strategic risks.
- Delivery report – to provide assurance on the delivery of regulatory activities.
- Development report – to provide assurance on the delivery of development activities.
- Deployment report – to provide an update on the deployment of resources.
The board meetings also provide the main means by which Board Members set the direction on issues of strategic importance that emerge over the course of the year.
The HTA’s Board is supported in its work by two standing committees:
- Audit and Risk Assurance Committee.
- Remuneration Committee.
- The Executive also holds quarterly accountability meetings with the Department of Health and Social Care to review progress with delivery of key performance indicators and the management of strategic risks.