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Centenary 1978
Lingua: Inglese
Editore: Worthing Baptist Church, United Kingdom, 1978
Da: RIVERLEE BOOKS, Waltham Cross, HERTS, Regno Unito
Valutazione del venditore 5 su 5 stelle
EUR 12,66
Spedizione EUR 13,81
Spedito da Regno Unito a U.S.A.Quantità: 1 disponibili
Aggiungi al carrelloSoft cover. Condizione: Good. Good for year paperback (staple binding): The book is in good readable condition 15 pages.
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![Immagine dell'editore per The Carcinogenicity Debate: Proceedings of a Workshop held at the Royal Society of Medicine, London, UK, April 1992 [CMR / Centre for Medicines Research Workshop Series] venduto da Tiber Books](https://pictures.abebooks.com/isbn/9781856420884-it-300.jpg)
The Carcinogenicity Debate: Proceedings of a Workshop held at the Royal Society of Medicine, London, UK, April 1992 [CMR / Centre for Medicines Research Workshop Series]
Lingua: Inglese
Editore: Quay Publishing, Lancaster, UK., 1992
ISBN 10: 1856420884 ISBN 13: 9781856420884
Da: Tiber Books, Cockeysville, MD, U.S.A.
Valutazione del venditore 4 su 5 stelle
Hardcover. Condizione: Very Good. 8vo, hardcover. No dj. Vg+ condition. Exterior faintly rubbed, contents bright, crisp & clean, virtually unopened. 286 pp.
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The Relevance of Ethnic Factors in the Clinical Evaluation of Medicines
Da: Zubal-Books, Since 1961, Cleveland, OH, U.S.A.
Valutazione del venditore 5 su 5 stelle
Condizione: Good. 284 pp., Hardcover, ex library, else text clean and binding tight. - If you are reading this, this item is actually (physically) in our stock and ready for shipment once ordered. We are not bookjackers. Buyer is responsible for any additional duties, taxes, or fees required by recipient's country.
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Timing of Toxicological Studies to Support Clinical Trials, The
Lingua: Inglese
Editore: Kluwer Academic Publishers, 1994
ISBN 10: 0792388720 ISBN 13: 9780792388722
Da: Fireside Bookshop, Stroud, GLOS, Regno Unito
Membro dell'associazione: PBFA
Valutazione del venditore 5 su 5 stelle
EUR 17,71
Spedizione EUR 28,65
Spedito da Regno Unito a U.S.A.Quantità: 1 disponibili
Aggiungi al carrelloCloth/Laminated Boards. Condizione: Very Good. Type: Book The timing of toxicological studies in relation to the clinical evaluation of new medicines is a key topic for strategic planners in the industry and those involved with harmonization. Resolving the anomalies between different regulatory authorities should eliminate redundant testing on animals and improve the efficiency of the developmental process by encouraging single international strategies. To aid industry in reaching a consensus, the Centre for Medicines Research has brought together representatives of the pharmaceutical industry from Europe, Japan and the USA to give a comprehensive account of current international industry positions on the subject. The contributions in this text review the situation and address the clinical and strategic requirements of the pre-clinical programme. Personal and consensus proposals on the toxicity studies required to initiate clinical investigations, the timing of reproductive toxicity tests and the duration of repeat-dose studies to support clinical development are provided. Small mark at base of spine.128pp.
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Improving the Regulatory Review Process: Assessing Performance and Setting Targets
Lingua: Inglese
Editore: Kluwer Academic Publishers, 1998
ISBN 10: 0792387317 ISBN 13: 9780792387312
Da: Fireside Bookshop, Stroud, GLOS, Regno Unito
Membro dell'associazione: PBFA
Valutazione del venditore 5 su 5 stelle
EUR 23,61
Spedizione EUR 28,65
Spedito da Regno Unito a U.S.A.Quantità: 1 disponibili
Aggiungi al carrelloCloth/Laminated Boards. Condizione: Very Good. Type: Book At a time when it is becoming usual for medicines to be developed for a global market and pharmaceutical companies are endeavouring to expedite the drug development process, Regulatory authorities are concentrating on improving their efficiency and effectiveness. Therefore, it is not surprising that questions are being asked as to how performance might be measured and compared between different authorities who are now often in receipt of dossiers that have been submitted to several agencies at the same time. Issues such as "what target should be set for the review of new medicines?" and "how can quality be assured?" are now considered to be of critical importance. The 12th CMR International Workshop, held in January 1997, provided the opportunity for regulatory authority and industry personnel from Europe, North America, Australia and Japan to openly discuss experiences and exchange views on how to improve the review process. The proceedings of this meeting provide a comprehensive overview of the current review process in different countries and the need for performance measures and targets. This volume summarizes the many suggestions that were debated at the workshop, and includes chapters on measuring performance, and on the integration of quality into the review process. 163pp.
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Relevance of Ethnic Factors in the Clinical Evaluation of Medicines : Proceedings of a Workshop Held at the Medical Society of London, Uk, 7th and 8th July, 1993
Da: GreatBookPrices, Columbia, MD, U.S.A.
Valutazione del venditore 5 su 5 stelle
EUR 52,40
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Improving the Regulatory Review Process : Assessing Performance and Setting Targets
Da: GreatBookPrices, Columbia, MD, U.S.A.
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EUR 52,40
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Improving the Regulatory Review Process: Assessing Performance and Setting Targets: Assessing Performance and Setting Targets (Centre for Medicines Research Workshop)
Da: California Books, Miami, FL, U.S.A.
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EUR 60,31
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The Relevance of Ethnic Factors in the Clinical Evaluation of Medicines: Proceedings of a Workshop held at The Medical Society of London, UK, 7th and ... 1993 (Centre for Medicines Research Workshop)
Da: California Books, Miami, FL, U.S.A.
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EUR 60,31
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Improving the Regulatory Review Process : Assessing Performance and Setting Targets
Da: GreatBookPrices, Columbia, MD, U.S.A.
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EUR 60,41
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The Relevance of Ethnic Factors in the Clinical Evaluation of Medicines: Proceedings of a Workshop held at The Medical Society of London, UK, 7th and ... 1993 (Centre for Medicines Research Workshop)
Da: Ria Christie Collections, Uxbridge, Regno Unito
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EUR 59,52
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Improving the Regulatory Review Process: Assessing Performance and Setting Targets: Assessing Performance and Setting Targets (Centre for Medicines Research Workshop)
Da: Ria Christie Collections, Uxbridge, Regno Unito
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EUR 59,52
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Improving the Regulatory Review Process
Da: Books Puddle, New York, NY, U.S.A.
Valutazione del venditore 4 su 5 stelle
Condizione: New. pp. xix + 163.
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Improving the Regulatory Review Process: Assessing Performance and Setting Targets (Centre for Medicines Research Workshop)
Da: Chiron Media, Wallingford, Regno Unito
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EUR 56,29
Spedizione EUR 17,75
Spedito da Regno Unito a U.S.A.Quantità: 10 disponibili
Aggiungi al carrelloPaperback. Condizione: New.
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The Relevance of Ethnic Factors in the Clinical Evaluation of Medicines (Centre for Medicines Research Workshop)
Da: Chiron Media, Wallingford, Regno Unito
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EUR 56,37
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Aggiungi al carrelloPaperback. Condizione: New.
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Improving the Regulatory Review Process : Assessing Performance and Setting Targets
Da: GreatBookPricesUK, Woodford Green, Regno Unito
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EUR 59,23
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Relevance of Ethnic Factors in the Clinical Evaluation of Medicines : Proceedings of a Workshop Held at the Medical Society of London, Uk, 7th and 8th July, 1993
Da: GreatBookPricesUK, Woodford Green, Regno Unito
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EUR 59,31
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The Relevance of Ethnic Factors in the Clinical Evaluation of Medicines: Proceedings of a Workshop Held at the Medical Society of London, Uk, 7th and (Paperback or Softback)
Da: BargainBookStores, Grand Rapids, MI, U.S.A.
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Paperback or Softback. Condizione: New. The Relevance of Ethnic Factors in the Clinical Evaluation of Medicines: Proceedings of a Workshop Held at the Medical Society of London, Uk, 7th and. Book.
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Improving the Regulatory Review Process : Assessing Performance and Setting Targets
Da: GreatBookPricesUK, Woodford Green, Regno Unito
Valutazione del venditore 5 su 5 stelle
EUR 65,45
Spedizione EUR 17,19
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Improving the Regulatory Review Process: Assessing Performance and Setting Targets (Centre for Medicines Research Workshop)
Da: Revaluation Books, Exeter, Regno Unito
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EUR 76,69
Spedizione EUR 11,46
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Aggiungi al carrelloPaperback. Condizione: Brand New. 1997 edition. 163 pages. 9.45x6.30x0.43 inches. In Stock.
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Improving the Regulatory Review Process: Assessing Performance and Setting Targets (Centre for Medicines Research Workshop)
Da: Ria Christie Collections, Uxbridge, Regno Unito
Valutazione del venditore 5 su 5 stelle
EUR 91,92
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The Relevance of Ethnic Factors in the Clinical Evaluation of Medicines (Centre for Medicines Research Workshop)
Da: Ria Christie Collections, Uxbridge, Regno Unito
Valutazione del venditore 5 su 5 stelle
EUR 91,92
Spedizione EUR 13,73
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Timing of Toxicological Studies to Support Clinical Trials
Da: GreatBookPrices, Columbia, MD, U.S.A.
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EUR 119,42
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Spedito in U.S.A.Quantità: Più di 20 disponibili
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EUR 50,35
Spedizione EUR 70,00
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. The Relevance of Ethnic Factors in the Clinical Evaluation of Medicines | Proceedings of a Workshop held at The Medical Society of London, UK, 7th and 8th July, 1993 | S. R. Walker (u. a.) | Taschenbuch | xviii | Englisch | 2013 | Springer | EAN 9789401046213 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
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EUR 50,35
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Improving the Regulatory Review Process: Assessing Performance and Setting Targets | N. McAuslane (u. a.) | Taschenbuch | Centre for Medicines Research Workshop | xix | Englisch | 2012 | Springer | EAN 9789401060424 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
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EUR 58,39
Spedizione EUR 61,56
Spedito da Germania a U.S.A.Quantità: 1 disponibili
Aggiungi al carrelloTaschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - At a time when it is becoming usual for medicines to be developed for a global market and pharmaceutical companies are endeavouring to expedite the drug development process, Regulatory Authorities are concentrating on improving their efficiency and effectiveness. Therefore, it is not surprising that questions are being asked as to how performance might be measured and compared between different authorities who are now often in receipt of dossiers that have been submitted to several agencies at the same time. Issues such as 'what target should be set for the review of new medicines ' and `how can quality be assured ' are now considered to be of critical importance. The twelfth CMR International Workshop, held in January 1997, provided the opportunity for Regulatory Authority and industry personnel from Europe, North America, Australia and Japan to openly discuss experiences and exchange views on how to improve the review process. The proceedings of this meeting provide a comprehensive overview of the current review process in different countries and the need for performance measures and targets. This volume summarises the many suggestions that were debated at the Workshop, and includes chapters on measuring performance, and on the integration of quality into the review process.
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The Relevance of Ethnic Factors in the Clinical Evaluation of Medicines : Proceedings of a Workshop held at The Medical Society of London, UK, 7th and 8th July, 1993
Lingua: Inglese
Editore: Springer, Springer Netherlands, 2012
ISBN 10: 9401046212 ISBN 13: 9789401046213
EUR 59,97
Spedizione EUR 62,29
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - For a research-based pharmaceutical company to be successful in the 1990s. it must have a strategic plan for the global development of new chemical entities. Global development can be defined as an attempt to reach all major markets as rapidly as possible and for many companies these will include the United States. Japan. Germany. France. Italy. UK and Canada. which together represent approximately 85% of the pharmaceutical market in the developed world. The mutual acceptance of foreign clinical data would reduce the time and resources required to develop a new medicine for the international market by eliminating the requirement for the routine repetition of clinical studies in local populations. In Japan this has been largely based on the belief that genetic differences in respon siveness may result in a different benefit/risk assessment for a new mediCine. while requests in Europe and the United States for local data relate mainly to methodological and cultural considerations. The importance of this issue has been recognised internationally as it was one of the topics discussed at the International Conference on Harmonisation in Orlando (October 1993) and it is currently on the programme for ICH3 which will be convened in Yokohama in Japan in November 1995.
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The Timing of Toxicological Studies to Support Clinical Trials
Da: Ria Christie Collections, Uxbridge, Regno Unito
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EUR 113,49
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The Timing of Toxicological Studies to Support Clinical Trials (CMR Workshop)
Da: Ria Christie Collections, Uxbridge, Regno Unito
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EUR 113,49
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Timing of Toxicological Studies to Support Clinical Trials
Da: GreatBookPrices, Columbia, MD, U.S.A.
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EUR 128,87
Spedizione EUR 2,27
Spedito in U.S.A.Quantità: Più di 20 disponibili
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