More than twenty programmes across six academic schools — fellowships, professional diplomas, executive certificates, workshops and vocational training.
Every programme sits within an academic school with a named lead responsible for its curriculum, teaching and assessment. Jump to a school below, or use the filter to search the whole catalogue.
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Fellowship programmes for clinicians and clinical pharmacists, spanning specialist therapeutics, acute and long-term care, and supervised international clinical experience.
Diagnosis and classification of diabetes, pharmacotherapy and insulin initiation, technology-assisted glucose management, obesity and dyslipidaemia, and structured complications screening within a multidisciplinary team.
Nutritional assessment and screening, therapeutic and modified diets, enteral and parenteral nutrition support, nutrition in chronic and critical illness, and counselling for sustained behaviour change.
Comprehensive geriatric assessment, frailty and falls, polypharmacy and deprescribing, cognitive impairment and delirium, continence, rehabilitation and advance care planning.
Resuscitation and trauma care, acute presentations across body systems, triage and departmental flow, procedural skills, and decision-making under time and resource pressure.
Medication error taxonomy and reporting, high-alert medicines, safe prescribing and administration systems, medication reconciliation, and root cause analysis of drug-related harm.
Antimicrobial resistance mechanisms, stewardship programme design, prospective audit and feedback, de-escalation and IV-to-oral switch, and measurement of stewardship outcomes.
Pharmacotherapy of the critically ill: sedation and analgesia, vasoactive support, sepsis management, therapeutic drug monitoring, nutrition and dosing in organ dysfunction and renal replacement.
Evidence-based management of acute coronary syndromes, heart failure, arrhythmia and anticoagulation, lipid and hypertension therapeutics, and cardiovascular risk reduction.
Cytotoxic, targeted and immunotherapy regimens, safe handling and dose verification, toxicity management, supportive care, and pharmacist-led counselling in the cancer pathway.
Acute, chronic and cancer pain assessment, multimodal and opioid therapy, opioid stewardship and tapering, neuropathic pain agents, and interventional and non-pharmacological adjuncts.
Antimicrobial pharmacokinetics and dynamics, treatment of major infection syndromes, resistant organisms, outpatient parenteral therapy, and infection in the immunocompromised host.
A structured, supervised clinical placement with a partner institution, supported by defined learning outcomes, a reflective portfolio and an end-of-placement supervisor report.
Professional diplomas and fellowship training across the pharmaceutical industry value chain — research, safety, regulation, medical affairs and scientific communication.
Trial design and protocol development, ICH-GCP and regulatory frameworks, informed consent, site selection and monitoring, data integrity, and the practical conduct of clinical studies.
Adverse event identification and coding, causality assessment, individual case safety reports, signal detection and risk management planning, and epidemiological methods for safety studies.
Regulatory and scientific writing: clinical study reports, protocols, investigator brochures, manuscripts and lay summaries, with reporting guidelines and publication ethics.
The medical affairs function: medical science liaison practice, scientific exchange, advisory boards, evidence generation planning, and compliant engagement with healthcare professionals.
Global regulatory pathways, dossier structure and the Common Technical Document, submissions and lifecycle management, labelling, and interaction with regulatory agencies.
The full development pathway from discovery to post-marketing: clinical development strategy, benefit–risk assessment, health authority interaction, and medical governance in industry.
Case intake and triage, MedDRA coding, narrative writing, expedited and periodic reporting timelines, and quality checks within a safety database.
Site-level trial conduct: feasibility, recruitment and consent, visit scheduling, source documentation, investigational product accountability and monitoring visits.
CRF design, database build and validation, data entry and query management, medical coding dictionaries, reconciliation and database lock.
Fellowships for professionals leading quality, safety and digital transformation within hospitals and health services.
Improvement science and measurement, accreditation standards and survey readiness, incident reporting and investigation, human factors, clinical audit, and building a culture of safety.
Electronic health records and interoperability standards, clinical decision support, data governance and security, analytics for service improvement, and the safe adoption of digital and AI-enabled tools.
Applied training in the economics and outcomes evidence that underpins health policy, reimbursement and priority setting.
Economic evaluation methods, cost-effectiveness and budget impact modelling, patient-reported and real-world outcomes, and the evidence requirements of reimbursement and HTA bodies.
Workshops, certification and collaborative projects that build practical research capability — from framing a question to publishing the result.
Formulating an answerable question, choosing a study design, sampling and bias, measurement and validity, protocol writing, and preparing an ethics submission.
Descriptive and inferential statistics, choosing the right test, regression, survival analysis, and hands-on analysis with practical interpretation of output.
Protocol registration, search strategy design, screening and data extraction, risk-of-bias assessment, pooled effect estimation, heterogeneity and PRISMA reporting.
The ICH-GCP principles in practice: responsibilities of sponsor, investigator and monitor, informed consent, essential documents, safety reporting and inspection readiness.
Participation in multi-site research led by the Centre, with supervision, methodological support and defined authorship criteria for contributing learners.
Vocational and executive certificate programmes that prepare learners for specific clinical, technical and administrative roles in healthcare.
Principles of inheritance and risk assessment, family history taking, genetic testing pathways, and communicating results with sensitivity and informed consent.
Workplace hazard identification, exposure assessment and control, health surveillance, fitness-for-work assessment, and occupational health legislation and reporting.
Structured education for people with diabetes: self-monitoring, insulin technique, nutrition and activity, hypoglycaemia management, foot care and motivational counselling.
Venepuncture technique and order of draw, specimen handling and labelling, infection control and sharps safety, patient identification, and management of complications.
Correct lead placement and artefact reduction, operation of recording equipment, ambulatory and exercise testing support, and recognition of recordings needing urgent review.
Personal care and dignity, vital signs and basic observations, moving and handling, infection prevention, communication, record keeping and safeguarding.
Recognition of cardiac arrest, high-quality chest compressions and ventilation, safe defibrillation with an AED, choking management and effective handover.
Rhythm recognition and management of shockable and non-shockable arrest, airway and access, arrest drug therapy, peri-arrest arrhythmias, team leadership and post-arrest care.
Systematic paediatric assessment, recognition of respiratory failure and shock, paediatric arrest algorithms, weight-based drug dosing and post-resuscitation stabilisation.
Clinical terminology and documentation review, ICD and CPT coding conventions, casemix and reimbursement, coding audit and compliance.
Real-time clinical documentation, medical terminology, EHR navigation, note structure and accuracy, and confidentiality and scope of practice.
CRF design, database build and validation, data entry and query management, medical coding dictionaries, reconciliation and database lock.
Case intake and triage, MedDRA coding, narrative writing, expedited and periodic reporting timelines, and quality checks within a safety database.
Site-level trial conduct: feasibility, recruitment and consent, visit scheduling, source documentation, investigational product accountability and monitoring visits.
Imaging modalities and their indications, patient preparation and positioning, radiation safety and protection, image quality assessment and departmental workflow.
Systematic interpretation of the 12-lead ECG: rate, rhythm, axis and intervals, ischaemia and infarction patterns, chamber enlargement, and common life-threatening findings.
Guidance on international registration pathways, documentation and credential verification, examination and language requirements, CV and interview preparation for overseas roles.
Taught content is delivered through live online seminars, released as recordings the same day, and supported by case discussion. Practical and simulation components are delivered in person at partner facilities in scheduled blocks.
Assessment varies by programme and may include written examinations, structured clinical assessment, case portfolios, supervised logbooks, project work and reflective practice. Criteria are published at enrolment.
Successful learners receive an Institute award naming the programme, the school and the assessment completed, with digital verification available to employers and regulators.
Our academic advisers will look at your qualifications, registration status and career goals, and recommend a school and programme — including recognition of prior learning where it applies.
