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Genomic Medicine and Pharmacogenomics

Professional Resources

Royal Pharmaceutical Society (RPS)

The RPS Pharmacogenomics (PGx) Standards Resource supports prescribers to build and expand PGx competence, helping them to prescribe safely and effectively using PGx, ultimately improving patient outcomes through medicines optimisation. It should be used alongside the RPS Prescribing Competency Framework as an additional resource.

The resource can be used by any prescriber, in settings across the UK, at any point in their career to underpin professional responsibility for prescribing when using PGx information. It is for all regulators, professional bodies, education providers and healthcare organisations.

British Pharmacological Society and Royal College of Physicians

Personalised Prescribing – Using pharmacogenomics to improve patient outcomes, a report from the British Pharmacological Society and the Royal College of Physicians published 28 March 2022, calls for pharmacogenomic testing to be integrated fully, fairly and swiftly into the NHS.

Royal College of General Practitioners (RCGP)

The RCGP Genomic Medicine topic guide published in August 2025 explores part of the RCGP curriculum, Being a General Practitioner. It helps understand important issues relating to genomics in primary care by illustrating the key learning points with a case scenario and questions. It also contains tips and advice for learning, assessment and continuing professional development (CPD), including guidance on the knowledge relevant to this area of general practice.

The British Society for Genetic Medicine, Royal College of General Practitioners, Royal Pharmaceutical Society, British Pharmacological Society, UK Clinical Pharmacy Association have produced a position statement on (DTC-GT) direct to consumer genomic testing (DTC-GT) to support healthcare professionals working in primary care and community settings.

Royal College of Psychiatrists

The role of genetic testing in mental health settings report was published in October 2023.  It provides clinically relevant summaries of the current evidence base for genetic testing across a range of mental health conditions.

Royal College of Pathologists

Consent and confidentiality in genomic medicine - new guidance for health professionals (rcpath.org)

Guidance on consent and confidentiality has been published by the College, the Royal College of Physicians and the British Society for Genetic Medicine to help healthcare professionals through the complex ethical issues that arise in genomic medicine.

NICE

Familial Hypercholesterolaemia:  Nice Guidelines

Familial breast cancer:  NICE Guidance

Guidance on CYP2C19 genotype testing to guide clopidogrel use after ischaemic stroke or transient ischaemic attack

Centre of Excellence in Regulatory Science and Innovation in Pharmacogenomics (CERSI-PGx)

Universal CYP2C19 genotyping for clopidogrel prescribing

Clopidogrel is a vital antiplatelet agent used widely in the UK to prevent atherothrombotic events. However, because clopidogrel is a prodrug, it requires enzymatic conversion by the CYP2C19 enzyme to become active. Genetic variants in the CYP2C19 gene can significantly reduce or even abolish this conversion, leaving patients with “intermediate” or “poor” metaboliser phenotypes at higher risk of recurrent strokes or heart attacks.
To address this, the Centre of Excellence in Regulatory Science and Innovation in Pharmacogenomics (CERSI-PGx) has developed new clinical guidelines to help prescribers integrate pharmacogenetic testing into standard care.

Medicines and Healthcare Products Regulatory Agency (MHRA)

The Yellow Card Biobank is a collaboration between the  Medicines and Healthcare products Regulatory Agency  (MHRA) and  Genomics England . Its goal is to improve understanding of how a patient’s genetic makeup may increase their risk of harm from side effects of medications. The Biobank is currently recruiting patients who have experienced side effects from specific medicines for a research project called the Yellow Card Biobank study.
 

UK Clinical Pharmacy Association (UKCPA)

The UKCPA Handbook of Pharmacogenomics aims to support the use of pharmacogenetic results to optimise medicines by providing healthcare professionals with evidence-based advice and guidance in a simple and easy to use format. It is a free-to-access online resource.

Clinical Pharmacogenetics Implementation Consortium

The Clinical Pharmacogenetics Implementation Consortium is a reputable, internationally recognised, peer reviewed and evidence-based resource. However, be aware it is American and so the recommendations can sometimes be better aligned with FDA-licensed products.

NHS England

 NHS England Fit for the Future: 10 Year Health Plan for England

Genomics features prominently in the NHS 10-year Plan. NHSE have predicted that by 2035, genomics could play a role in up to half of all health encounters

 NHS England's Genomics Education Programme exists to deliver and advise on learning and development opportunities that prepare current and future NHS professionals to make the best use of genomics in their practice

 Nursing and midwifery genomics framework in England

This Nursing and midwifery genomics framework updated in September 2025  illustrates how nurses and midwives should be enabled and empowered to adopt genomics into their clinical practice.

 Implementing lynch syndrome testing and surveillance pathways

NHS South East Genomics

The South East Genomics Medicine Service delivers NHS genomic testing across Kent, Medway, Surrey, Sussex and South London covering a population of 8.5 million people.

Training and Education

The Centre of Excellence in Regulatory Science and Innovation in Pharmacogenomics (CERSI-PGx)

CERSI-PGx has officially launched a new e-learning portal designed to accelerate the adoption of pharmacogenomics (PGx) in real-world clinical practice.

Led by the University of Liverpool in partnership with the British Pharmacological Society (BPS) and Queen Mary University of London, the portal offers free, bitesized online learning tailored for healthcare and regulatory professionals. The platform aims to build confidence and capability in applying PGx to improve therapeutic outcomes.

NHS England Genomics Education Programme Genomics Education Programme - Genomics Education Programme (hee.nhs.uk)

NHS England’s Genomics Education Programme exists to deliver and advise on learning and development opportunities that prepare current and future NHS professionals to make the best use of genomics in their practice. Training resources include:

  • GeNotes (Quick, concise information to help healthcare professionals make the right genomic decisions at each stage of a clinical pathway)
  • Articles, Factsheets, videos, Podcasts
  • Teaching and clinical resources
  • Taught Courses, PGCert, PGDip, MSc
 

e-learning for health Genomics in the NHS – elearning for healthcare (e-lfh.org.uk)

The Genomics in the NHS programme is a collection of e-learning courses developed by NHS educational teams to support and educate healthcare professionals about genomic medicine and the benefit it will bring to patient care.

Royal College of General Practitioners (RCGP) Genomics toolkit Genomics toolkit: Introduction | RCGP Learning

The Genomics Toolkit has been developed in partnership with Health Education England Genomics Education Programme to support increasing understanding, raise awareness of Genomics Medicine and support primary care with increased knowledge of how genomics can contribute to improving patient care in a 'genomics era'. 

This toolkit is designed to be used by the entire clinical primary care team. It is a collection of resources that explain how Genomics Medicine can be incorporated in Primary Care, including training resources and audit suggestions, and providing links to relevant guidance and patient resources. The resources can be used as quick reference resources or as a package for CPD, to deliver awareness-raising and educational events, and in supporting trainees preparing for the MRCGP.

Future Learn The Genomics Era: The future of genomics in healthcare

An introduction to the growing role of genomics in healthcare, for patient diagnoses, treatment and disease prevention.

Centre for Pharmacy Postgraduate Education (CPPE) Genomics (cppe.ac.uk)

CPPE is a provider of educational solutions for the NHS pharmacy workforce across England to maximise its contribution to improving patient care. Genomic resources include:

  • Links to medicines related education and tools for genomics
  • Introduction to genomics in pharmacy e-learning package
  • Genomics in pharmacy: an introduction to person centred consultations e-learning package
 

Medicines Learning Portal Medicines Learning Portal: Pharmacogenomics

This tutorial has been specially commissioned by NHS England is to support all pharmacists, pharmacy technicians and trainees working in primary and/or secondary care who currently have limited experience working with pharmacogenomic information.

Pharmacy and Genomics-informed Medicines Optimisation Webinar Recording

The NHSE Pharmacy Workforce Group for Genomics held a webinar for all pharmacy professionals providing NHS services on Tuesday 9th September. Presenters included members of the NHS Genomic Medicine Service and NHSE National Genomics Education programme. The webinar provided an introductory overview for all pharmacy professionals on the area of genomics-informed medicines optimisation, including:

  1. What is genomics?
  2. What are the national priorities for genomics-informed medicines optimisation?
  3. How does genomics affect medicines? (Pharmacogenomics, precision medicines and antimicrobial resistance)
  4. Education opportunities for pharmacy professionals and introduction to the next webinar.

The webinar recording is now available on the pharmacy page for genomics education: 'Online courses, learning and resources' in the Link Bank.

Local Resources

Genomics and the NHS 10 year plan Surrey and Sussex January 2026 (please log in to the Learning Hub to view), please click here to view the accompanying slides.

Genomic Medicine in Primary Care and Pharmacogenomics with Dr Debbie Hipps, Primary Care lead SE Genomic Medicine Service Alliance, and Sarah Flack, Primary Care Pharmacist, Surrey Heartlands ICB. The video is protected, please contact Surrey Training Hub team for password.

Getting to Grips with Genomics Series for Primary Care (Surrey and Sussex Cancer Alliance & NHS SE Genomic Medicine Service)

ESR1 Breast ctDNA Testing Education Session - North Thames GMS : North Thames GMS

Patient Resources

Cancer websites

MacMillan:  Cancer genetics booklet | Macmillan Cancer Support

Cancer research UK:  Family History and Inherited Cancer Genes

Chemo-prevention for women with no history of breast cancer

Chemo-prevention:  NICE tamoxifen decision aid

Rare Disease websites

Genetic Alliance  is an umbrella organisation for 200 organisations, including Rare Disease UK, and Syndromes Without A Name, and support groups for individual rare diseases.  These provide information and support for patients and families affected by a genetic condition and are also a source of information and practical advice for healthcare professionals.

Unique  is a charity supporting and informing families with a rare chromosome disorder, and some single gene disorders. 

Unique also has a  list of guides  for healthcare professionals for individual chromosomal disorders (including deletions and duplications) in English and other languages.

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