Clinical Trials Handbook.pdf

Clinical Trials Handbook

Curtis L. Meinert

A systematic approach to all aspects of designing and conducting clinical trials The success or failure of clinical trials hinges on hundreds of details that need to be developed, often under less than ideal conditions. Written by one of the worlds leading trialists, Clinical Trials Handbook: Design and Conduct provides clinicians with a complete guide to designing, conducting, and evaluating clinical trials teaching them how to simplify the process and avoid costly mistakes. The author draws on his extensive clinical trials experience to outline all steps employed in setting up and running clinical trials, from budgeting and fundraising to publishing the results. Along the way, practical advice is offered while also addressing a mix of logistical, ethical, psychological, behavioral, and administrative issues inherent to clinical trials. Topics of coverage include: Protocols for drug masking, controls, and treatment randomization Consent, enrollment, eligibility, and follow-up procedures Different types of sample size design and data collection and processing Working with study centers, research staff, and various committees Monitoring treatment effects and performance, and ensuring quality control Data analysis and access policies for study data and documents Clinical Trials Handbook is invaluable for practicing clinicians and trialists who would like to learn more about or improve their understanding of the design and execution of clinical trials. The book is also an excellent supplement for courses on clinical trials at the graduate level.

Clinical Trials pertains to the design, development, safe conduct and interpretation of trials for therapeutic products in humans. This course is designed to provide students with the skills to interpret the clinical literature, understand Good Clinical Practice (GCP) and clinical development and give students the skills to design and analyse clinical trials from first time in man Phase I

1.75 MB DATEIGRÖSSE
ISBN
Englisch SPRACHE
Clinical Trials Handbook.pdf

Technik

PC und Mac

Lesen Sie das eBook direkt nach dem Herunterladen über "Jetzt lesen" im Browser, oder mit der kostenlosen Lesesoftware Adobe Digital Editions.

iOS & Android

Für Tablets und Smartphones: Unsere Gratis tolino Lese-App

Andere eBook Reader

Laden Sie das eBook direkt auf dem Reader im Hugendubel.de-Shop herunter oder übertragen Sie es mit der kostenlosen Software Sony READER FOR PC/Mac oder Adobe Digital Editions.

Reader

Öffnen Sie das eBook nach der automatischen Synchronisation auf dem Reader oder übertragen Sie es manuell auf Ihr tolino Gerät mit der kostenlosen Software Adobe Digital Editions.

Aktuelle Bewertungen

avatar
Sofia Voigt

OCT Handbook 2020

avatar
Matteo Müller

20.06.2017 · The selection of appropriate outcomes is crucial when designing clinical trials in order to compare the effects of different interventions directly. For the findings to influence policy and practice, the outcomes need to be relevant and important to key stakeholders including patients and the public, health care professionals and others making decisions about health … Welcome to the Clinical Handbook of …

avatar
Noel Schulze

Handbook for Clinical Trials - MODEPHARMA Handbook for Clinical Trials We have published a useful reference handbook intended to be a quick reference for all persons involved in planning and conducting clinical research. The following three documents have been selected for their importance and demand when planning a clinical trial with a particular focus on the investigational medicinal product:

avatar
Jason Lehmann

Clinical Trials pertains to the design, development, safe conduct and interpretation of trials for therapeutic products in humans. This course is designed to provide students with the skills to interpret the clinical literature, understand Good Clinical Practice (GCP) and clinical development and give students the skills to design and analyse clinical trials from first time in man Phase I

avatar
Jessica Kohmann

6 Jan 2020 ... Clinical trials require an application to the. Therapeutic Goods Administration ( TGA) under the Clinical Trial Notification (CTN) or Clinical Trial.