Find out more about the members of TAC D by reading their biographies.

Professor Gary McVeigh (Chair)

Professor of Cardiovascular Medicine, Queen's University Belfast and Consultant Physician, Belfast Health and Social Care Trust

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Gary is a Consultant Physician/Clinical Pharmacologist in the Belfast Health and Social Care Trust and Professor of Cardiovascular Medicine at Queen's University Belfast. Gary qualified from Queen's University and trained in Belfast and Minneapolis, USA.

His major clinical and academic interests relate to cardiovascular complications associated with hypertension, diabetes mellitus and hyperlipidaemia. He has served as a member of the Executive Committee of the British Hypertension Society and is currently a member of the Guidelines and Information Committee. Gary was Regional Advisor for Northern Ireland and member of council for the Royal College of Physicians of Edinburgh. Gary chairs the Drugs and Therapeutics and New Drugs Committees and is the lead clinician for Therapeutic reviews in the Belfast Trust. He is the Training Programme Director for Clinical Pharmacology and Therapeutics in Northern Ireland.

Gary was former Vice Chair of Technology Appraisal Committee C and is currently Standing Chair of an internal Guideline Development Group for NICE.


Dr Lindsay Smith, BSc MClinSci PhD MD FRCP FRCGP FHEA (Vice Chair)

General Practitioner, Westlake Surgery, Somerset

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Lindsay Smith has been a General Practitioner in Somerset for over 25 years. During this time he has undertaken primary care research through both academic departments and research general practices. He has previously been a Consultant senior lecturer in general practice and primary care. Currently he is an honorary senior lecturer at Bristol University, a CCG Patient Safety Lead.

He has previously worked for NICE as a member of its TA appeals committee, its QOF advisory committee and various GDGs. Additionally he has been a member of its Quality Standards Advisory Committee, its CG Rapid Updates Standing Committee and a member of its Suspected Cancer GDG.


Dr Nabeel Alsindi

GP Clinical Lead for Primary care, Doncaster CCG

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Nabeel has worked as a General Practitioner and Commissioner in Doncaster since 2014. He qualified from Oxford University in 2009 and has worked in various hospitals and GP surgeries across Sheffield and Doncaster.

After finishing his GP training, Nabeel undertook a Commissioning Fellowship. This has led to a permanent role with Doncaster Clinical Commissioning Group as Clinical Lead for Primary Care and Long Term Conditions. He sits on the CCG's Primary Care Commissioning Committee and provides a wider primary care perspective into a number of forums both within and external to the CCG. He is also a member of the Yorkshire & Humber Clinical Senate Assembly.


Dr Aomesh Bhatt

Director of Regulatory and Medical Affairs, Europe and North America, Reckitt Benckiser

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Biography to follow.


Professor David Bowen, MA MB BChir MD MRCP FRCPath

Consultant Haematologist, Leeds Teaching Hospitals NHS trust

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David qualified from Cambridge University and Middlesex Hospital, London. He trained in Haematology in London and Cardiff, with first his Consultant appointment in Dundee,then in Leeds where he has worked since 2005. His clinical expertise is in myeloid malignancies, with research interests in the etiology, molecular basis and clinical trial management of these diverse and rare cancers.

He has chaired the National Cancer Research Institute Myelodysplastic Syndromes (MDS) subgroup and the British Committee for Standards in Haematology Guideline group for MDS. He co-chairs the European Myelodysplastic Syndrome Registry programme, accruing data for clinical effectiveness of management interventions in community-based practice.


Dr Matthew Bradley

Therapy Area Leader, Global Health Outcomes, GlaxoSmithKline

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Matt is Vice President, Therapy Area Head for Value Evidence & Outcomes at GlaxoSmithKline. Prior joining GSK, Matt was a Value Demonstration Leader for AstraZeneca Global Research and Development. He has previously been responsible for the coordination and delivery of an integrated programme of HTA across the Sanofi-Aventis portfolio in the UK and has also worked for Pfizer. Prior to moving into the Pharmaceutical Industry he was a Senior Research Fellow at the NHS Centre for Reviews and Dissemination (CRD), a lead reviewer for the Cochrane Collaboration, an author of strategic reports for the NHS HTA programme, the Department of Health and the Prime Minister's Office (UK Government).

Matthew has previously chaired the Association of British Pharmaceutical Industries TDA User Group, been a peer reviewer for the NHS HTA programme and sat on the New Medicines Group (NMG) for the All Wales Medicines Strategy Group.


Susan Dutton

Senior Medical Statistician, Oxford Clinical Trials Research Unit

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Susan is a senior medical statistician and the lead statistician of the Oxford Clinical Trials Research Unit (OCTRU), a UKCRC Registered Clinical Trials Unit. The scope of OCTRU is to design, conduct and report in both early and later phase clinical trials in surgery, musculoskeletal sciences, respiratory medicines, gastroenterology and oncology including development pathways and the evaluation of new health technologies in surgery and interventional procedures; trauma, rehabilitation and conservative management; respiratory medicine/intervention and randomised trials; pharmaceuticals, particularly in oncology; the management of inflammation; and biomarkers to refine treatment strategies.

Susan has a BSc in Mathematics from Durham University and an MSc in Biometry from the University of Reading. She has worked as a medical statistician within academia and has experience in the design, analysis and reporting of various clinical trials and epidemiological studies. Susan joined the Centre for Statistics in Medicine at the University of Oxford in January 2007 to work as part of a team of medical statisticians providing statistical support for clinical trials in oncology. In 2013 Susan was appointed to be the Statistical Lead of the Oxford Clinical Trials Research Unit (OCTRU). Susan provides statistical input into a variety of Phase I-IV clinical trials from providing advice early in the development of the research, through designing the trial for grant application, through set-up, data collection, analysis and publication. Susan provides statistical oversight of trials and staff in OCTRU. Susan also participates in the methodological research undertaken by the Centre for Statistics in Medicine.


Professor Rachel Elliott

Professor of Health Economics, University of Manchester

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Biography to follow


Gillian Ells, BPharm PGDip MSc

Prescribing Advisor - Commissioning. Hastings and Rother Clinical Commissioning Group and Eastbourne, Hailsham and Seaford Clinical Commissioning Group

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Gillian Ells is a pharmacist working for two clinical commissioning groups on the south east coast of England. Her previous experience includes working in both the hospital and the community sector.

She has spent the past 16 years in primary care as a pharmaceutical advisor and now specialises in the commissioning of new drug treatments and management of the local health economy drug formulary. Gillian has recently completed a Masters in Health Economics and Health Policy at Birmingham University.


Professor Paula Ghaneh

Professor and Honorary Consultant Surgeon, University of Liverpool

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Paula Ghaneh is a Professor of Surgery at the University of Liverpool and an Honorary Consultant Surgeon at the Royal Liverpool University Hospital.

Her clinical specialty is hepato-pancreato-biliary surgery. Her research interests are pancreatic cancer and clinical trials. She is the Deputy Director of the Cancer Research UK Liverpool Cancer Trials Unit. She is a member of the NCRI upper GI CSG and pancreatic cancer subgroup.


Dr Peter Hall

Senior Clinical Lecturer in Medical Oncology, University of Edinburgh

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Peter Hall is an academic Medical Oncologist with a research interest in and Health Economics and Health Technology Assessment in Cancer. He treats patients with breast cancer at the Edinburgh Cancer Centre and leads the Health Economics Group within the University of Edinburgh Clinical Trials Unit.

He graduated from the University of Edinburgh Medical School in 2003, undertaking general medical training in Fife and Dundee then specialist training in Medical Oncology with the Yorkshire Deanery in 2006. He undertook at NICE scholarship in 2007 and completed a PhD in Health Economics and Clinical Trial design at the University of Leeds in 2012.

The focus of his research is on the development of improved methods for efficient research design, cost-effectiveness analysis and the measurement of clinical and socioeconomic outcomes using data obtained from research and routinely collected within the NHS.


Rebecca Harmston

Lay Member

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Rebecca works as an independent public and patient adviser for a number of universities and research institutions within the UK. She is a member of both PPIREs and INSPIRE, which are Norfolk-based public and patient involvement groups involved in scientific research and mental health projects. Rebecca sits on a number of research committees as a Lay Member including the Health Technology Assessment Women and Child's Health Panel, the Research for Patient Benefit East of England Committee and is also a member of the NHS Patient and Public Voices Group.

Rebecca has a strong interest in medical and scientific research and a background in academic research, scientific review and ethics. She has completed a PhD and Masters by Research degree in Biological Sciences, and has worked as a Scientific Officer for Cancer Research UK for seven years and Biochemistry at Cambridge University for three years.


Sumithra Maheswaran, MPharm (Hons) MBA MRPharmS

Trust Pharmacist, London Ambulance Service NHS Trust

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Biography to follow


Dr David Meads

Associate Professor, Health Economics, University of Leeds

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David Meads is a health economist in the Academic Unit of Health Economics, University of Leeds. He has many years of experience conducting economic evaluations alongside clinical trials, decision-analytic modelling and stated preference studies. David leads the Economic Evaluation for HTA module on the AUHE Health Economics MSc and supervises several PhD students. He regularly contributes to the NIHR Research Design Service.


Malcolm Oswald

Lay member

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Malcolm works as an independent consultant. His background is in systems analysis, analysing what people and organisations providing health care do and also what information they need to do it. Since the late 1990s, he has specialised in information governance, working mostly for National bodies in England and Scotland specifying the rules that control who accesses confidential patient information in systems. This involves interpreting and applying law and policy, consulting clinicians and patient/public representatives.

Malcolm has completed a PhD in Bioethics and Medical Jurisprudence. His thesis explores how, in a democracy, we should decide how resources are allocated to health care, analysing competing theories from philosophy, economics and other disciplines. In 2011, he co-authored the Royal College of General Practitioners' guidance on ethical commissioning (“Making Difficult Choices”).


Professor Oluwafemi Oyebode

Professor of Psychiatry & Consultant Psychiatrist, The National Centre for Mental Health

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Femi graduated in Medicine in 1977. He has been Consultant Psychiatrist in Birmingham since 1986. He is currently Professor of Psychiatry at the University of Birmingham.

He is on the Editorial Boards of the British Journal of Psychiatry, the Psychiatric Bulletin and Advances in Psychiatric Treatment. His research interests include Clinical Psychopathology, Medical Humanities and Medical Ethics.


Dr Paula Parvulescu, MD MSc MPH FFPH

Consultant in Public Health Medicine, Liverpool City Council

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Paula is a Consultant in Public Health Medicine specialised in healthcare public health, working for Liverpool City Council. In her role, she works with NHS commissioners to make sure that a population health approach is undertaken and pathways and models of care are based on best available evidence.

Paula trained as a Public Health Physician in Romania and holds a MSc degree in Health Policy, Economics and Management from Maastricht University in the Netherlands. In her previous roles, Paula worked as a health economics and outcomes research consultant and in academia as a public health lecturer.


William Turner

Consultant Urologist, Cambridge University Hospitals NHS Foundation Trust

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Bill is one of three urologists in a specialist multidisciplinary team based in Cambridge. He trained in surgery in general and then in urology, in the UK and in Switzerland, in particular in bladder cancer and in reconstructive urology.

He has been Clinical Lead for Urology at Addenbrooke’s, Training Programme Director for Urology for East Anglia, and a member of the Cambridge Research Ethics Committee. He is currently the East of England Regional Representative on the Council of the British Association of Urological Surgeons.

He has previously been a member of Technology Appraisal Committees C and A, a member of the NICE Male Lower Urinary Tract Symptoms Guideline Development Group, clinical lead for the NICE Guideline Development Group on the Diagnosis and Treatment of Bladder Cancer, a member of the European Association for Urology Guideline Development Group on Incontinence and a member of the International Consultation on Urological Diseases consultations on BPH and on Bladder Cancer.


More information

Find out more about the committee and read papers from previous meetings.

About the Technology Appraisal committee

 

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