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Therapeutic Risk Management of Medicines (Woodhead Publishing Series in Biomedicine) de Anjan Banerjee,Stephen Mayall,Steve Mayall

Descripción - Críticas '...a must-have book for those working in the field of therapeutic risk management of medicines...very useful as a training book for new pharmacovigilance officers, but it is also useful for experienced staff…' --Drug Safety, Oct 2014 Reseña del editor Summary New medicines have always had risks as well as benefits but, until recently, the majority of major drug safety catastrophes arose unpredictably, often with devastating public health consequences. Many potentially useful drugs have also had approvals delayed or refused due to inadequate benefit risk planning and mitigation. Risk management plans are compulsory for new drug filings in Europe since 2004, and in the US for selected drugs a REMS (Risk Evaluation and Mitigation Strategies) is needed. The legislation has evolved rapidly over the last decade and Therapeutic risk management of medicines is an authoritative, and yet practical guide on planning, writing, implementing and evaluating risk management plans for medicines globally. Chapters are also included on the historical development, lessons from other industries, the regulatory and health authority perspective and public communication of benefit risk. This topic is of critical importance not only to the pharmaceutical and biotechnology industry, but also prescribers, pharmacists, regulators and healthcare policymakers. About the Authors Dr Stephen J. Mayall is a senior consultant at Pope Woodhead & Associates. He has over 13 years of consulting and project management experience within the global pharmaceutical industry, and has been involved in therapeutic risk management since 2003. Steve has worked on the development and/or implementation of over 25 risk management plans, including EU-RMPs, REMS, RiskMAPs and developmental-stage RMPs. These have covered a diverse range of therapeutic areas, product types, life cycle stages and client companies. Steve has a Bachelor's degree in natural sciences (biochemistry) from the University of Cambridge, and a PhD in cell biology awarded by University College London for work performed in the laboratory of a Nobel Prize winner. Dr Anjan 'Swapu' Banerjee is Pope Woodhead & Associates (Cambridgeshire, UK) Deputy Managing Director and Head of Regulatory and Risk Management Practice. He has wide experience of over 40 global risk management programmes, is a member of the ENCePP network of EMA and has been involved in multiple EU and US regulatory filings, regulatory projects and the design of clinical development programmes. He is also a Faculty member in Regulatory, Drug safety and Risk management at the Institute of Biotechnology, Cambridge University, has published widely in the field, and has supervised over 10 Mphil students from this programme. Swapu joined Pope Woodhead from Roche where he was a Global Drug Safety Scientist (Physician). Swapu has over 15 years' experience in global pharmaceuticals, biotech and devices (clinical development, medical marketing), and more than 30 years' experience in healthcare, as well as being a practising Hon. Consultant General and Colorectal surgeon in the NHS. Swapu is medically qualified with a higher research doctorate equivalent, has finance training (Securities Institute) and is MBA, FRCP(Edin), FRCS(Gen), FRCS(Glas), FAcadMEd, FICS, MFPM and is an FSB. Contents Introduction and historical background of risk management plans; EU-RMP (Risk Management Plan); USA REMS (Risk Evaluation and Mitigation Strategies); Safety specification; Pharmacovigilance planning; Assessing the need for risk minimization; Risk minimization tools; Implementation of RMPs and REMS; Evaluation of RMPs and REMS; Developmental risk management plans; Effectively negotiating with the health authorities; Public communication of benefit risk. Biografía del autor Dr Stephen Mayall is a Principal Consultant at Pope Woodhead & Associates. He has over 15 years of consulting and project management experience in the global pharmaceutical industry, and has focused on therapeutic risk management since 2003. Steve has worked on the development and/or implementation of over 40 risk management plans, including EU-RMPs, REMS and development-stage RMPs. These have encompassed a diverse range of therapeutic areas, product types, life-cycle stages and client companies. He has also conducted a variety of other consulting projects for global pharmaceutical and biotechnology companies, covering communications, drug safety, clinical development, strategic marketing and in-licensing topics. This broader experience has provided valuable insights for placing risk management in a wider context within different organisations and healthcare systems. Steve has a Bachelor’s degree in natural sciences (biochemistry) from the University of Cambridge, and a PhD in cell biology from University College London.Dr Anjan “Swapu” Banerjee is Deputy Managing Director (Deputy CEO) of Pope Woodhead & Associates and Head of Development Consulting. He has wide experience of numerous global risk management programmes, is a member of the ENCePP network and has been involved in multiple EU and US regulatory filings, regulatory projects and the design of clinical development programmes. He is also a Faculty member in Regulatory, Drug Safety and Risk Management at the Institute of Biotechnology, Cambridge University. Anjan has over 15 years of experience in global pharmaceuticals, biotech, advanced therapies and devices in clinical development, regulatory, medical affairs and drug safety roles in addition to experience as a Management Consultant at McKinsey & Company. He has spent more than 30 years in healthcare, remaining clinically active as a part-time Honorary Consultant Surgeon at Bedford Hospital NHS Trust. He has completed UK higher medical training in pharmaceutical medicine (as well as general surgery) and has an MSc in pharmacoepidemiology. Anjan is MBBS, DM, MBA, FRCP(Edin), FRCS(Gen), FRCS(Glas), FAcadMEd, FICS, MFPM, FSB.

Therapeutic risktaking a justifiable choice bjpsych promoting therapeutic risktaking can be complex professionals can experience tension striving for a balance between the interests of the individual and societal pressures to control risk this article examines therapeutic risktaking, recognising the challenges to supporting it in practice and debating how they may be overcome Fundamentals of risk management understanding, evaluating this fifth edition of fundamentals of risk management is a comprehensive introduction to commercial and business risk for students and risk professionals providing extensive coverage of the core frameworks of business continuity planning, enterprise risk management and project risk management, this is the definitive guide to dealing with the different types of risk an organization faces Therapeutic risk management of medicines woodhead therapeutic risk management of medicines is an authoritative and practical guide on developing, implementing and evaluating risk management plans for medicines globally it explains how to assess risks and benefitrisk balance, design and roll out risk minimisation and pharmacovigilance activities, and interact effectively with key stakeholders

Therapeutic risk management of medicines ebook, 2014 get this from a library therapeutic risk management of medicines stephen j mayall anjan k banerjee therapeutic risk management of medicines is an authoritative and practical guide on developing, implementing and evaluating risk management plans for medicines globally it explains how to assess Libro fundamentals of risk management 9780749479619 fundamentals of risk management hopkin, paul fundamentals of risk management, now in its fourth edition, is a comprehensive introduction to commercial and business risk for students and a broad range of risk professionals providing extensive coverage of the core frameworks of business continuity planning, enterprise risk Risk management una nueva forma de asegurar el exito risk management una nueva forma de asegurar el exito profesional de fancesc roses envío gratis en 1 día desde 19 libro nuevo o segunda mano, sinopsis, resumen y opiniones

Detalles del Libro

  • Name: Therapeutic Risk Management of Medicines (Woodhead Publishing Series in Biomedicine)
  • Autor: Anjan Banerjee,Stephen Mayall,Steve Mayall
  • Categoria: Libros,Libros universitarios y de estudios superiores,Medicina y ciencias de la salud
  • Tamaño del archivo: 9 MB
  • Tipos de archivo: PDF Document
  • Idioma: Español
  • Archivos de estado: AVAILABLE


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Descarga gratuita de risk management tools free edition gratis descarga fiable para windows pc de risk management tools free edition gratis descarga libre de virus y 100 limpia consigue risk management tools free edition descargas alternativas Therapeutics and clinical risk management dove press issn 11766336 print went to online only in 2009 an international, peerreviewed open access journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines, therapeutic and surgical interventions in all clinical areas Therapeutic risk management of medicines 1st edition therapeutic risk management of medicines is an authoritative and practical guide on developing, implementing and evaluating risk management plans for medicines globally it explains how to assess risks and benefitrisk balance, design and roll out risk minimisation and pharmacovigilance activities, and interact effectively with key stakeholders

Erfolgsfaktor risikomanagement 30 methoden, beispiele erfolgsfaktor risikomanagement 30 methoden, beispiele, checklisten praxishandbuch für industrie und handel romeike, frank, hager, peter libros en Therapeutic risk management of medicines sciencedirect therapeutic risk management of medicines is an authoritative and practical guide on developing, implementing and evaluating risk management plans for medicines globally it explains how to assess risks and benefitrisk balance, design and roll out risk minimisation and pharmacovigilance activities, and interact effectively with key stakeholders Heads of medicines agencies risk management the united kingdom uk withdrew from the european union eu on 31 january 2020 and is no longer an eu member statehma and cmdhv are in the process of making appropriate changes to this website if the site still contains content that does not yet reflect the withdrawal of the uk from the eu, this is unintentional and will be addressedin case you notice information that should be updated


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