CIP Exam Workbook

CIP Exam Workbook

Author: Pramod Lad

Publisher:

Published: 2018-06-10

Total Pages: 244

ISBN-13: 9781720934028

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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 responsivities 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 4 (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.


CIP Exam Workbook

CIP Exam Workbook

Author: Pramod Lad

Publisher:

Published: 2018-09-02

Total Pages: 244

ISBN-13: 9781726273671

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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.


Institutional Review Board

Institutional Review Board

Author: Elizabeth A. Bankert

Publisher: Jones & Bartlett Learning

Published: 2006

Total Pages: 568

ISBN-13: 9780763730499

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This comprehensive reference covers three separate areas related to IRBs: administration, daily management; and ethical issues. This instructional manual provides IRB members and administrators with the information they need to run an efficient and effective system of protecting human research subjects, while remaining in compliance with federal research regulations. The text includes case studies, sample forms, and sample policy documents. The updated Second Edition includes seven new chapters: IRB Closure of Study Files, Internet Research, Research in Public Schools, Phase I Clinical Trials in Healthy Volunteers, Vulnerability in Research, Balancing the Risks and Potential Benefits,and HIPAA.


Cip Exam Study Guide

Cip Exam Study Guide

Author: Pramod M. Lad

Publisher:

Published: 2019-02-03

Total Pages: 269

ISBN-13: 9781795730549

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PRODUCT DESCRIPTION This study guide provides one tool for the preparation and study for the CIP examination. It is a companion book to the CIP Exam Workbook. The sequence of chapters in the study guide follows the same sequence as in the CIP exam workbook and the flow of ideas in each chapter is concordant with the sequence of questions in the workbook. It is recommended that the two books be studied together for the most effective exam preparation. The study guide is organized in distinct chapters each of which covers one aspect of the regulations or guidances. The study material is designed to instruct on core information relevant to the examination. However it is hoped that the study guide can also function as an IRB Handbook. The study guide is therefore designed not only to prepare for the CIP examination but also to educate IRB professionals and Clinical Research Coordinators on matters which arise frequently in IRB administration. 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 responsivities 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.The book addresses the key issues in federal regulations outlined in statutes including Title 45 part 4 (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.


Institutional Review Board Member Handbook

Institutional Review Board Member Handbook

Author: Robert J. Amdur

Publisher: Jones & Bartlett Publishers

Published: 2010-10-22

Total Pages: 224

ISBN-13: 1449609929

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The Essential Resource for All IRB Members! Designed to give Institutional Review Board (IRB) members the information they need to protect the rights and welfare of research subjects in a way that is both effective and efficient, the chapters of the Institutional Review Board Member Handbook are short and to the point. Topic-specific chapters list the criteria IRB members should use to determine how to vote on specific kinds of studies and offer practical advice on what IRB members should do before and during full-committee meetings. NEW CHAPTERS in this Edition Include: * Definition of Human Subject Research, Exempt & Expedited Review Categories * IRB Member Conflict of Interest All chapters are completely updated for 2010 practice! This handbook is an excellent accompaniment to Institutional Review Board: Management and Function, Second Edition and the Study Guide that IRB members can access and refer to quickly and easily.


CISSP: Certified Information Systems Security Professional Study Guide

CISSP: Certified Information Systems Security Professional Study Guide

Author: James Michael Stewart

Publisher: John Wiley & Sons

Published: 2011-01-13

Total Pages: 927

ISBN-13: 1118028279

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Totally updated for 2011, here's the ultimate study guide for the CISSP exam Considered the most desired certification for IT security professionals, the Certified Information Systems Security Professional designation is also a career-booster. This comprehensive study guide covers every aspect of the 2011 exam and the latest revision of the CISSP body of knowledge. It offers advice on how to pass each section of the exam and features expanded coverage of biometrics, auditing and accountability, software security testing, and other key topics. Included is a CD with two full-length, 250-question sample exams to test your progress. CISSP certification identifies the ultimate IT security professional; this complete study guide is fully updated to cover all the objectives of the 2011 CISSP exam Provides in-depth knowledge of access control, application development security, business continuity and disaster recovery planning, cryptography, Information Security governance and risk management, operations security, physical (environmental) security, security architecture and design, and telecommunications and network security Also covers legal and regulatory investigation and compliance Includes two practice exams and challenging review questions on the CD Professionals seeking the CISSP certification will boost their chances of success with CISSP: Certified Information Systems Security Professional Study Guide, 5th Edition.


Ccrp Exam Workbook

Ccrp Exam Workbook

Author: Pramod Lad

Publisher:

Published: 2018-10-09

Total Pages: 258

ISBN-13: 9781726836081

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Clinical research management including the management of clinical trials is a complex activity involving several different individuals with varying educational and professional backgrounds. Research investigators, clinical research coordinators, research nurses, monitors, IRB staff, regulatory personnel, to name a few, all play an important role in clinical trial and clinical research management. . The Society of Clinical Research Associates (SOCRA) provides an important forum for the education, and training of clinical research professionals. A significant component of this training is the certification exam which results in the CCRP (Certified Clinical Research Professional) designation. This designation is particularly important to clinical research coordinators and research nurses who provide the main site-associated support for clinical trial and clinical research management. The certification serves as an important milestone in career development and can assist clinical research coordinators in careers in both academic and teaching hospitals, CROS, as well as within the pharmaceutical industry.The examination evaluates knowledge, understanding, and application of the conduct of clinical research and clinical trials involving humans. It tests the familiarity with "the International Conference on Harmonisation Guideline for Good Clinical Practice (E6) (ICH/GCP), ICH Clinical Safety Data Management: Definitions and Standards for Expedited Reporting (E2A), the United States Code of Federal Regulations (CFR) and the ethical principles that guide clinical research consistent with the principles of the Nuremberg Code, the Belmont Report and the Declaration of Helsinki."This workbook provides one tool for the preparation and study for the CCRP examination. The book addresses the key issues in in ICH-GCP , 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 CCRP exam covers material based not only on these regulations but also on guidances issued by OHRP and the FDA 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 than offering linguistically ingenious choices. The workbook is therefore designed not only to prepare for the CCRP examination but also to educate clinical research professionals, particularly clinical research coordinators and research nurses on matters which arise frequently in clinical research management and administration.


Current Catalog

Current Catalog

Author: National Library of Medicine (U.S.)

Publisher:

Published: 1993

Total Pages: 1628

ISBN-13:

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First multi-year cumulation covers six years: 1965-70.


CERTIFIED INFORMATION PROFESSIONAL (AIIM IQ0-100) Exam Practice Questions and Dumps

CERTIFIED INFORMATION PROFESSIONAL (AIIM IQ0-100) Exam Practice Questions and Dumps

Author: Books Fortune

Publisher: Books Fortune

Published: 2020-09-16

Total Pages: 48

ISBN-13:

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AIIM worked with industry experts and focus groups to define the body of understanding necessary for information professionals to be successful in the Intelligent Information Management era and built a certification exam based upon this body of knowledge. Here we’ve brought best Exam practice questions for you so that you can prepare well for AIIM exam. Unlike other online simulation practice tests, you get an Ebook version that is easy to read & remember these questions. You can simply rely on these questions for successfully certifying this exam.


CBIC Study Guide

CBIC Study Guide

Author: Trivium

Publisher: TTPP

Published: 2020-10-16

Total Pages: 278

ISBN-13: 9781635308662

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Updated for 2021, Trivium Test Prep's unofficial, NEW CBIC Study Guide: Exam Book with Practice Test Questions for the Certification Board of Infection Control and Epidemiology Examination isn't your typical exam prep! Because we know your time is limited, we've created a product that goes beyond what most study guides offer. With CBIC Study Guide, you'll benefit from a quick but total review of everything tested on the exam with current, real examples, graphics, and information. These easy to use materials give you that extra edge you need to pass the first time. Certification Board of Infection Control and Epidemiology, Inc. was not involved in the creation or production of this product, is not in any way affiliated with Trivium Test Prep, and does not sponsor or endorse this product. Trivium Test Prep's CBIC Study Guide offers: A full review of what you need to know for the CBIC exam Practice questions for you to practice and improve Test tips to help you score higher Trivium Test Prep's CBIC Study Guide covers: IDENTIFYING INFECTIOUS DISEASES SURVEILLANCE, ANALYSIS, AND CHANGE OCCUPATIONAL HEALTH PROGRAMS LEADERSHIP, MANAGEMENT AND COMMUNICATION EDUCATION ...and includes a FULL practice test! About Trivium Test Prep Trivium Test Prep is an independent test prep study guide company that produces and prints all of our books right here in the USA. Our dedicated professionals know how people think and learn, and have created our test prep products based on what research has shown to be the fastest, easiest, and most effective way to prepare for the exam. Unlike other study guides that are stamped out in a generic fashion, our study materials are specifically tailored for your exact needs. We offer a comprehensive set of guides guaranteed to raise your score for exams from every step of your education; from high school, to college or the military, to graduate school. Let our study guides guide you along the path to the professional career of your dreams!