Isbn: 9780471988243 - conducting gcp-compliant clinical research (20 resultados)

Hardcover. Condición: Very Good. 1. It's a well-cared-for item that has seen limited use. The item may show minor signs of wear. All the text is legible, with all pages included. It may have slight markings and/or highlighting.

hardcover. Condición: New. In shrink wrap. Looks like an interesting title.

HRD. Condición: New. New Book. Shipped from UK. Established seller since 2000.

Condición: new.

Condición: New.

Condición: New.

Condición: As New. Unread book in perfect condition.

Condición: As New. Unread book in perfect condition.

Condición: New. In English.

Hardback. Condición: New. 1st. Bei der Entwicklung und klinischen Prüfung neuer Wirkstoffe muß in allen Stadien entsprechend der GCP (guten klinischen Praxis) vorgegangen werden. Dieses Buch richtet sich besonders an Anfänger auf dem Gebiet der pharmazeutisch-klinischen Forschung; es erklärt die Grundlagen der GCP vereinfacht und gut nachvollziehbar. Mögliche Fehler und ihre Folgen werden anhand von Fallstudien anschaulich erläutert. Mit zahlreichen Literaturhinweisen. (06/99).…

Condición: New.

Gebunden. Condición: New. Conducting GCP-Compliant Clinical Research Wendy Bohaychuk and Graham Ball Good Clinical Research Practices, UK and Canada The overall aim of this work is to provide a reference book which describes the general framework for conducting GCP-compliant clinica.

Condición: New. The overall aim of this work is to provide a reference book which describes the general framework for conducting GCP-compliant clinical research, particularly pharmaceutical industry clinical research. It is designed to accommodate both those new to the business and the more experienced. Num Pages: 226 pages, black & white illustrations. BIC Classification: GBC; KNDP; MBGR; MJ; MMG. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 240 x 162 x 20. Weight in Grams: 490. . 1999. 1st Edition. Hardcover. . . . .…

Hardback. Condición: New. 1st. Bei der Entwicklung und klinischen Prüfung neuer Wirkstoffe muß in allen Stadien entsprechend der GCP (guten klinischen Praxis) vorgegangen werden. Dieses Buch richtet sich besonders an Anfänger auf dem Gebiet der pharmazeutisch-klinischen Forschung; es erklärt die Grundlagen der GCP vereinfacht und gut nachvollziehbar. Mögliche Fehler und ihre Folgen werden anhand von Fallstudien anschaulich erläutert. Mit zahlreichen Literaturhinweisen. (06/99).…

Hardcover. Condición: Brand New. 1st edition. 226 pages. 9.75x6.25x0.75 inches. In Stock.

Buch. Condición: Neu. Neuware - Conducting GCP-Compliant Clinical Research Wendy Bohaychuk and Graham Ball Good Clinical Research Practices, UK and Canada The overall aim of this work is to provide a reference book which describes the general framework for conducting GCP-compliant clinical research, particularly pharmaceutical industry clinical research. Wendy Bohaychuk and Graham Ball run a consultancy, GCRP Ltd., which has conducted over 820 GCP audits involving more than 200 companies in the last 10 years. More than 5,000 individuals have been involved in their training courses to help people perform GCP-compliant clinical research. They have authored several books and articles including: Standard operating procedures for investigators Standard operating procedures for sponsors and CROs GCP - an indexed reference Drawing on their wealth of experience, they have produced this enlightening and practical reference work which fills an educational gap in the understanding of GCP at all levels. Written in concise language simple enough to be accessible to those new in the field, the dozens of real-life stories and detailed case studies at the end of each chapter make the book an invaluable resource for the more experienced, highlighting what can go wrong in a clinical study: A study of prostate cancer in the UK - An investigator brochure was not provided. The company argued that a brochure was unnecessary because the drug was already marketed. Indeed it was - for hypertension! A study of cardiovascular surgery in the UK - The consent dates were changed (by overwriting) to indicate that the patients had provided consent before the study started. The original dates post-dated the start of the study. A study of hypertension in Germany - The investigator brochure predated the study by nine years! Checklists are provided throughout the book to help monitors, auditors and investigators ensure that nothing important is overlooked. The authors present the topic of GCP with remarkable clarity, insight and enthusiasm emphasizing that this code of practice was not designed to make studies more difficult for investigators or more expensive for sponsors and CROs but, in the final analysis, to ensure the safety and well-being of study participants and future patients who will benefit from well-conducted, GCP-compliant studies.; Bei der Entwicklung und klinischen Prüfung neuer Wirkstoffe muß in allen Stadien entsprechend der GCP (guten klinischen Praxis) vorgegangen werden. Dieses Buch richtet sich besonders an Anfänger auf dem Gebiet der pharmazeutisch-klinischen Forschung; es erklärt die Grundlagen der GCP vereinfacht und gut nachvollziehbar. Mögliche Fehler und ihre Folgen werden anhand von Fallstudien anschaulich erläutert. Mit zahlreichen Literaturhinweisen. (06/99). …

Condición: New. The overall aim of this work is to provide a reference book which describes the general framework for conducting GCP-compliant clinical research, particularly pharmaceutical industry clinical research. It is designed to accommodate both those new to the business and the more experienced. Num Pages: 226 pages, black & white illustrations. BIC Classification: GBC; KNDP; MBGR; MJ; MMG. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 240 x 162 x 20. Weight in Grams: 490. . 1999. 1st Edition. Hardcover. . . . . Books ship from the US and Ireland.…

Hardcover. Condición: new. Hardcover. Conducting GCP-Compliant Clinical Research Wendy Bohaychuk and Graham Ball Good Clinical Research Practices, UK and Canada The overall aim of this work is to provide a reference book which describes the general framework for conducting GCP-compliant clinical research, particularly pharmaceutical industry clinical research. Wendy Bohaychuk and Graham Ball run a consultancy, GCRP Ltd., which has conducted over 820 GCP audits involving more than 200 companies in the last 10 years. More than 5,000 individuals have been involved in their training courses to help people perform GCP-compliant clinical research. They have authored several books and articles including: Standard operating procedures for investigatorsStandard operating procedures for sponsors and CROsGCP - an indexed reference Drawing on their wealth of experience, they have produced this enlightening and practical reference work which fills an educational gap in the understanding of GCP at all levels. Written in concise language simple enough to be accessible to those new in the field, the dozens of real-life stories and detailed case studies at the end of each chapter make the book an invaluable resource for the more experienced, highlighting what can go wrong in a clinical study: A study of prostate cancer in the UK - An investigator brochure was not provided. The company argued that a brochure was unnecessary because the drug was already marketed. Indeed it was - for hypertension! A study of cardiovascular surgery in the UK - The consent dates were changed (by overwriting) to indicate that the patients had provided consent before the study started. The original dates post-dated the start of the study. A study of hypertension in Germany - The investigator brochure predated the study by nine years! Checklists are provided throughout the book to help monitors, auditors and investigators ensure that nothing important is overlooked. The authors present the topic of GCP with remarkable clarity, insight and enthusiasm emphasizing that this code of practice was not designed to make studies more difficult for investigators or more expensive for sponsors and CROs but, in the final analysis, to ensure the safety and well-being of study participants and future patients who will benefit from well-conducted, GCP-compliant studies. The overall aim of this work is to provide a reference book which describes the general framework for conducting GCP-compliant clinical research, particularly pharmaceutical industry clinical research. It is designed to accommodate both those new to the business and the more experienced. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.…

Condición: New. pp. 226 This item is printed on demand.

Hardcover. Condición: Brand New. 1st edition. 226 pages. 9.75x6.25x0.75 inches. In Stock. This item is printed on demand.