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It is important to be aware of the legal and ethical frameworks within which research is undertaken and of the steps that are available to prevent fraudulent and dishonest research being undertaken and written up. This book, originally put together by Stephen Lock, an editor of the British Medical Journal, and now revised extensively by Michael Farthing, editor of the gastroenterology journal Gut, provides an overview of the entire topic. Background material on the regulatory frameworks, in North America as well as Europe, is laid out in detail, and the history of fraud and misconduct is illustrated admirably by contributions from Stephen Lock and Frank Wells, a co-editor and expert in ethical and legal issues relating to the pharmaceutical industry. A series of slightly less riveting accounts of individual country’s approaches to research fraud follows, with the best chapters coming towards the end, where personal experiences are used to illuminate the devastating effects that involvement in research fraud can have for patients and practitioners. Michael Farthing has contributed an excellent editorial view on research misconduct to conclude the book.

Medicine --- Physicians --- Médecine --- Médecins --- Research. --- Malpractice. --- Recherche --- Responsabilité professionnelle --- wetenschapsethiek (wetenschappelijk wangedrag, fraude) --- biomedisch, medisch-wetenschappelijk onderzoek --- éthique de la science (inconduite scientifique) --- recherche biomédicale --- Médecine --- Médecins --- Responsabilité professionnelle

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Ethics, Medical --- Informed Consent --- Consent (Law) --- Informed consent (Medical law) --- Medical ethics --- Consentement (Droit) --- Ethique médicale --- legislation & jurisprudence --- geïnformeerde vrijwillige toestemming (instemming) --- biomedisch, medisch-wetenschappelijk onderzoek --- Frankrijk --- consentement libre et éclairé --- recherche biomédicale --- France --- Consentement éclairé (Droit médical) --- Éthique médicale --- Expérimentation humaine en médecine --- Aspect moral --- Ethique médicale --- Expérimentation humaine en médecine - Aspect moral

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Biotechnologies enable us to be smarter, have better memories be stronger and quicker, live longer, be more resistant to diseases, and enjoy richer emotional lives. Buchanan explores urgent ethical issues raised by these developments, about what it is to be human and what sort of society we should strive to have.

Medical innovations --- Moral and ethical aspects. --- biomedisch, medisch-wetenschappelijk onderzoek --- biomedische technologie --- menselijke natuur --- verbetergeneeskunde (mensverbetering) --- rechtvaardigheid (rechtvaardigheidsprincipe, distributieve rechtvaardigheid) --- ethiek (ethische aspecten) --- recherche biomédicale --- technologie biomédicale --- nature humaine --- médecine de l'amélioration (médecine d'amélioration) --- justice (principe de justice, justice distributive, justice sociale) --- ethique (aspects ethiques) --- Biomedical Enhancement --- Innovations, Medical --- Medicine --- Medical technology --- Technological innovations --- Moral and ethical aspects --- Innovations --- Medical law --- Professional ethics. Deontology --- Médecine --- Aspect moral --- ethics. --- Medical innovations - Moral and ethical aspects.

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This highly engaging guide for clinical researchers provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical research. It includes practical information on ethical principles in clinical research, designing appropriate research studies, writing consent and assent documents, getting protocols approved, special populations, confidentiality issues, and the reporting of adverse events. A valuable appendix includes a listing of web resources about research ethics as well as a glossary. This will be an invaluable resource for basic

Clinical Protocols. --- Ethics. --- Writing. --- Biomedical Research --- Clinical trials. --- Etudes cliniques --- ethics. --- Clinical Protocols --- Proposal writing in medicine --- Human experimentation in medicine --- standards --- ethics --- Moral and ethical aspects --- biomedisch, medisch-wetenschappelijk onderzoek --- onderzoeksprotocol --- recherche biomédicale --- protocole de recherche --- Authorship --- Medical writing --- Controlled clinical trials --- Patient trials of new treatments --- Randomized clinical trials --- Trials, Clinical --- Clinical medicine --- Research --- Medical protocols. --- Clinical algorithms --- Clinical protocols --- Patient care plans --- Plans for patient care --- Protocols in medicine --- Medical records --- Clinical Protocols - standards --- Biomedical Research - ethics --- Human experimentation in medicine - Moral and ethical aspects

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Represents the results of PRIVIREAL, an EC-funded project, examining the implementation of Directive 95/46/EC on data protection in relation to medical research and the role of ethics committees in European countries. This volume relates to the project's second stage, and is for those concerned with data protection issues in medical research. "The Data Protection and Medical Research in Europe: PRIVIREAL" series represents the results of this EC-funded project examining the implementation of Directive 95/46/EC on data protection in relation to medical research and the role of ethics committees in European countries. The series consists of five separate volumes following the complete development of the PRIVIREAL project. This volume relates to the second stage of this project and is concerned with the setting up and role of research ethics committees. It assesses their legal responsibilities, especially with regard to data protection matters and contains reports from more than 20 European countries on these issues. Focusing on the theoretical role and practical operation of research ethics committees and the impact of relevant international and national instruments, this volume will be an essential resource for all those concerned with data protection issues in medical research.

Medical records --- Data protection --- Medicine --- Law and legislation --- Research --- 342.721 <4> --- ethische commissies --- biomedisch, medisch-wetenschappelijk onderzoek --- medisch dossier --- Europa --- Persoonlijke vrijheid. Privacy. Wetgeving i.v.m. transplantatie van organen--Europa --- comités d'éthique --- recherche biomédicale --- dossiers médicaux --- Europe --- 342.721 <4> Persoonlijke vrijheid. Privacy. Wetgeving i.v.m. transplantatie van organen--Europa --- Clinical sciences --- Medical profession --- Human biology --- Life sciences --- Medical sciences --- Pathology --- Physicians --- Clinical records --- Health records --- Hospital medical records --- Patient care records --- Communication in medicine --- Hospital records --- Health Workforce --- Medical records - Law and legislation - European Union countries --- Data protection - Law and legislation - European Union countries --- Medicine - Research - Law and legislation - European Union countries --- Dossiers médicaux --- Protection de l'information (Informatique) --- Médecine --- Droit --- Recherche