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OverviewThis book is designed to serve as a guide for the clinical trial investigator who is willing to initiate clinical study from their own. The chapters include Basics of IITs, IIT and Regulation, IIT and Association with Industry, Protocol Designing, Budget Preparation, Case Report Form, Informed Consent, Reporting, Clinical Trial Registration, EC Submission, Conduct and Monitoring, Data Management, CSR Preparation etc. Each chapter is thoughtfully developed to simplify the job of a clinical trial investigator. Full Product DetailsAuthor: T C GeorgePublisher: Createspace Independent Publishing Platform Imprint: Createspace Independent Publishing Platform Dimensions: Width: 17.80cm , Height: 0.60cm , Length: 25.40cm Weight: 0.200kg ISBN: 9781540762894ISBN 10: 1540762890 Pages: 106 Publication Date: 01 December 2016 Audience: General/trade , General Format: Paperback Publisher's Status: Active Availability: In stock  We have confirmation that this item is in stock with the supplier. It will be ordered in for you and dispatched immediately. Table of ContentsReviewsAuthor InformationDr T C George has been engaged in clinical trial operations for more than 14 years. He has been a part of 120+ clinical trials at various positions. He started his career as Clinical Research Coordinator (CRC) and then appraised to as Clinical Trial Monitor in a short span of time. For a long time he has also worked as a freelancer for various sponsor and CROs as a Clinical Trial Monitor. Presently he is working as an Operations-Manager. Tab Content 6Author Website:Countries AvailableAll regions |
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