HIPAA and Human Subjects Research: A Question & Answer Reference Guide (March 2003)

- $24.95

This publication, HIPAA and Human Subjects Research: A Question & Answer Reference Guide (March 2003), by Mark Barnes and Jennifer Kulynych of Ropes & Gray, quickly and conveniently access all of the essential clinical trial-related HIPAA regulations and guidance documents - and analysis and perspectives from the two leading HIPAA experts - all in one pocket-sized handbook! Learn how HIPAA will affect all aspects of clinical research --patient recruitment, informed consent, IRB reviews, clinical data handling, and the responsibilities of sponsors, IRBs, monitors, and investigators-- in this definitive reference guide designed and developed by the top HIPAA experts! This essential guide is more than just your personal HIPAA Privacy Rule library: We've supplemented all the key HIPAA privacy-related documents by having our experts answer over 100 of the most common, emerging, and difficult-to-answer HIPAA-related questions now facing clinical trial sponsors, study monitors, clinical investigators and site staff, IRBs, and others affected by the HIPAA Privacy Rule. Check out the table of contents (TOC) to see the sections found in this book. Call for bulk discounts. 5.5"x7" spiral-bound pocket guide. 139 pages. ISBN # 1-882615-66-2


LinkedIn twitter Facebook 

On-Demand GCP Refresher Training 

Too busy to attend a course? Our newly-released GCP eLearning course may be your solution!
For details on our scenario-based practical GCP application on-demand course, click here.

GCP for Investigators

Barnett’s scenario-based eLearning course is designed with the busy Principal Investigator in mind.  Based on real-life scenarios encountered by investigative site teams, this highly focused 7-module GCP training is designed to ensure comprehensive understanding of the key components of GCP.

For more details on this scenario-based eGCP program for investigators please click here. 

BARNETT CATALOG The Barnett Catalogue is your comprehensive guide to the myriad live, web, and custom training opportunities offered throughout the year. 

Jan - July 2014 Edition

Winter CatalogDownload Today!  

Blended Curriculum Path for the CRA, CRC, and Project Manager

BCP Cover

Download Today! 






 View Catalog of Offerings   

New Titles added every month! 
Course Alumni Save 50% 


Monitoring Clinical Drug Studies: Intermediate 

Informed Consent Content & Process Requirements for Biobanking Studies 

Auditing Techniques for Clinical Research Professionals 


10-Week CRA & CRC Beginner Program  

Trial Master File (TMF) for Sponsors: Set-Up and Maintenance 

Use of Notes to File in Clinical Trial Essential Documentation 

10-Week Clinical Research Associate (CRA) On-Boarding Program  


2012 GCP Question & Answer Guide Print Edition 

2012 Good Clinical Practice Question & Answer Guide Electronic Edition 

CFR/ICH GCP Reference Guide 2012 (Spiral Bound) 

CFR/ICH GCP Reference Guide 2012 (Perfect Bound) 

PAREXEL's Bio/Pharma R&D Statistical Sourcebook 2012/2013 (Hard Copy)