9781726273671-1726273679-CIP Exam Workbook

CIP Exam Workbook

ISBN-13: 9781726273671
ISBN-10: 1726273679
Edition: Second Edition
Author: Pramod M Lad
Publication date: 2018
Publisher: CreateSpace Independent Publishing Platform
Format: Paperback 244 pages
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Book details

ISBN-13: 9781726273671
ISBN-10: 1726273679
Edition: Second Edition
Author: Pramod M Lad
Publication date: 2018
Publisher: CreateSpace Independent Publishing Platform
Format: Paperback 244 pages

Summary

CIP Exam Workbook (ISBN-13: 9781726273671 and ISBN-10: 1726273679), written by authors Pramod M Lad, was published by CreateSpace Independent Publishing Platform in 2018. With an overall rating of 4.5 stars, it's a notable title among other books. You can easily purchase or rent CIP Exam Workbook (Paperback) from BooksRun, along with many other new and used books and textbooks. And, if you're looking to sell your copy, our current buyback offer is $0.3.

Description

PRODUCT DESCRIPTION The Institutional Review Board (IRB) is responsible for the review of a wide variety of clinical research. As the complexity of clinical research has grown over the years, the duties and responsibilities of the IRB have grown increasingly complex. This complex environment demands that the IRB be staffed and managed by professionals. As a part of affirming the professionalism of IRB staff, administrators and directors, the Public Responsibility in Research and Medicine (PRIM&R) provides an important forum for education and affirmation of ethical standards for the performance and management of clinical research. An important component of this program is the certification exam known as the CIP (Certified IRB Professional). This examination, which is offered twice a year, covers a wide range of regulatory topics. This workbook provides one tool for the preparation and study for the CIP examination. The book addresses the key issues in federal regulations outlined in statutes including Title 45 part 46 (Protection of Human Subjects) , Title 21 part 50 ( Protection of Human Subjects), Title 21 part 56 (Institutional review Boards) Title 21 part 54 (Financial Disclosures by Clinical Investigators) . Also addressed are key FDA statutes involved in the regulation of clinical trials Title 21 part 312 (Investigational New Drug Application), Tile 21 part 812 (Investigational Device Exemptions) and Title 21 part 11(Electronic Records and Electronic Signatures). The CIP exam covers material based not only on these regulations but also on guidances issued by OHRP and the FDA. Special attention has been devoted to material covered in these guidances. Also addressed are interactions of the IRB with other committees in the institutional environment. Some of the material also covers ICH guidelines for clinical trial management. The workbook is organized in distinct chapters each of which covers one aspect of the regulations or guidances. The multiple choice questions are deliberately designed to instruct on core materials rather offering linguistically ingenious choices. An answer key is provided. The workbook is therefore designed not only to prepare for the CIP examination but also to educate IRB professionals on matters which arise frequently in IRB administration.
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