Comprehensive practical guide clinical (15 Ergebnisse)

Zustand: Good. Pages intact with minimal writing/highlighting. The binding may be loose and creased. Dust jackets/supplements are not included. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.

Paperback. Zustand: Very Good. The book has been read, but is in excellent condition. Pages are intact and not marred by notes or highlighting. The spine remains undamaged.

paperback. Zustand: Very Good. The Comprehensive Guide To Clinical Research: A Practical Handbook For Gaining Insight Into The Clinical Research Industry This book is in very good condition and will be shipped within 24 hours of ordering. The cover may have some limited signs of wear but the pages are clean, intact and the spine remains undamaged. This book has clearly been well maintained and looked after thus far. Money back guarantee if you are not satisfied. See all our books here, order more than 1 book and get discounted shipping.…

Taschenbuch. Zustand: Sehr gut. Gebraucht - Sehr gut Leichte Lagerspuren -A Comprehensive and Practical Guide to Clinical Trials provides an overview of the entire process of clinical research in one thorough and easy-to-read handbook that offers those involved in clinical research a clear understanding of how the components of a study are related. It focuses on the practical aspects of the preparation and execution of a clinical trial and offers tools and resources to help the entire team understand how their responsibilities tie together with the tasks and duties of other members. This allows for better planning and prioritization, and can lead to more effective and successful clinical trials. With practical examples, checklists and forms, this book is a useful guide for planning and conducting clinical trials from beginning to end. 210 pp. Englisch.…

Paperback. Zustand: Very Good. Shipped within 24 hours from our UK warehouse. Clean, undamaged book with no damage to pages and minimal wear to the cover. Spine still tight, in very good condition. Remember if you are not happy, you are covered by our 100% money back guarantee.

Zustand: New. In English.

Paperback. Zustand: Very Good. No Jacket. Former library book; May have limited writing in cover pages. Pages are unmarked. ~ ThriftBooks: Read More, Spend Less.

Taschenbuch. Zustand: Neu. Neuware.

Taschenbuch. Zustand: Neu. Neuware - Master the latest updates and principles of ICH GCP E6(R3) with this indispensable guide for clinical research professionals. This comprehensive resource provides a clear and practical exploration of the ICH GCP E6(R3) guideline, equipping professionals with the tools and insights needed to excel in clinical research. From foundational principles to the latest advancements in trial design and data management, this guide is your essential companion for navigating the complexities of modern clinical studies. Topics covered in this book include: - Introduction to ICH GCP E6(R3): Understand the evolution and importance of GCP in clinical research.- Investigator and Sponsor Responsibilities: Key obligations to ensure compliance, participant safety, and trial success.- Ethics and IRB/IEC Oversight: Safeguard participant rights and maintain ethical standards throughout the trial.- Digital and Computerized Systems: Strategies for secure data management and regulatory compliance in the digital age.- Monitoring, Auditing, and Risk Management: Proactive approaches to quality assurance and issue resolution.- Protocol Development and Essential Records: Practical guidance for effective documentation and operational excellence.- Annex 2 Insights: Adapt GCP principles to decentralized, pragmatic, and real-world data trials.Whether you're a seasoned professional or new to clinical research, this book offers actionable guidance, real-world examples, and clarity on ICH GCP E6(R3)'s key updates. Elevate your expertise, prioritize participant welfare, and ensure trial integrity with this essential resource. Perfect for: - Clinical Research Professionals- Investigators and Sponsors- Regulatory and Compliance Specialists- IRB/IEC Members- Anyone who has an interest in Clinical Research Regulatory TopicsPrepare to lead with confidence in the ever-evolving world of clinical research. Pick up your copy of ICH - GCP E6(R3) Comprehensive Resource Guide for Clinical Research Professionals: Practical Insights and Key Updates for Clinical Study Design and Application right now.…

Paperback. Zustand: Brand New. 1st edition. 196 pages. 9.00x6.00x0.50 inches. In Stock.

paperback. Zustand: Sehr gut. 210 Seiten; 9780128047293.2 Gewicht in Gramm: 500.

Paperback. Zustand: Brand New. 1st edition. 196 pages. 9.00x6.00x0.50 inches. In Stock.

Taschenbuch. Zustand: Neu. A Comprehensive and Practical Guide to Clinical Trials | Delva Shamley (u. a.) | Taschenbuch | Englisch | 2017 | Elsevier Science | EAN 9780128047293 | Verantwortliche Person für die EU: Kolibri 360 GmbH, Ettore-Bugatti-Str. 6-14, 51149 Köln, produktsicherheit[at]kolibri360[dot]de | Anbieter: preigu. …

Zustand: New. 2017. 1st Edition. Paperback. Editor(s): Shamley, Delva (School of Health Care, Headington, Oxford). Num Pages: 224 pages. BIC Classification: MBN; MMG. Category: (P) Professional & Vocational. Dimension: 229 x 152. . . . . . . Books ship from the US and Ireland.

Kartoniert / Broschiert. Zustand: New. Describes the entire clinical trial management process from start to finish in a step-by-step guideProvides best practice elements, including case studies, practical examples, activities, and checklistsRedaktion: Delva Sha.