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Showing 1 - 17 of 17 results for Bernard Naughton
Transformation2: leading a mega-project turnaround(opens in new window)
- Chapter
- Megaproject Leaders: Reflections on Personal Life Stories
Major Programme Management
Technology and Operations Management
COVID-19 and risks to the supply and quality of tests, drugs, and vaccines(opens in new window)
- Journal article
- Lancet Global Health
Global access to quality-assured medical products: the Oxford Statement and call to action(opens in new window)
- Journal article
- Lancet Global Health
Responsible innovation and commercialisation in the university context: a case study of an academic entrepreneur in digital healthcare(opens in new window)
- Chapter
- Responsible Innovation in Digital Health
Traceability and Supply Chain
- Journal article
- Regulatory Affairs Professionals Society
International Counterfeit Medicine Regulation
- Journal article
- Naughton B, Koshkouei M, Smith J, Brindley, D, Jacob C: International Counterfeit Medicine Regulation. Chapter 7 in Fundamentals of International Regulatory Affairs 3rd Edition, 2017. Regulatory Affairs Professionals Society.
The EU Falsified Medicines Directive: key implications for dispensers(opens in new window)
- Journal article
- Medicine Access @ Point of Care
International Counterfeit Medicines Regulation
- Chapter
- Fundamentals of International Regulatory Affairs
Medicine authentication technology as a counterfeit medicine-detection tool: a Delphi method study to establish expert opinion on manual medicine authentication technology in secondary care(opens in new window)
- Journal article
- BMJ Open
Health Care
Organisation Studies
Effectiveness of medicines authentication technology to detect counterfeit, recalled and expired medicines: a two-stage quantitative secondary care study.(opens in new window)
- Journal article
- BMJ Open
Health Care
Organisation Studies
The European Falsified Medicines Directive in Poland: background, implementation and potential recommendations for pharmacists(opens in new window)
- Journal article
- European Journal of Hospital Pharmacy
EU Falsified Medicines Directive mandatory requirements for secondary care: A concise review(opens in new window)
- Journal article
- Journal of Generic Medicines
Health Care
Organisation Studies
The limitations of QALY: a literature review(opens in new window)
- Journal article
- Journal of Stem Cell Research and Therapy
Health Care
Organisation Studies
Establishing good authentication practice (GAP) in secondary care to protect against falsified medicines and improve patient safety.(opens in new window)
- Journal article
- European journal of hospital pharmacy. Science and practice
J.A. Smith, B. Naughton, A. Kramm, G. Smith, A. Ohanjanyan, M. De Simone, R. Horne and D.A. Brindley. European Union Falsified Medicines Directive: Requirements and Implications for Multi-Stakeholder Healthcare Delivery. Chapter 8 in Fundamentals of EU Regulatory Affairs 7th Edition. Regulatory Affairs Professionals Society.
- Chapter
- Fundamentals of EU Regulatory Affairs 7th Edition. Regulatory Affairs Professionals Society.