Get answers to "Frequently Asked Questions" on HIPAA in Clinical Trials: A Practical Guide for Research Compliance
Download the PDF today. The HIPAA privacy compliance date has come and gone. You need a resource that'll help you ensure your researchers are complying with HIPAA regulations. You also need to ensure that your researchers apply HIPAA regulations together with existing Food and Drug Administration (FDA) and Common Rule research regulations.
The book and companion CD-ROM, HIPAA in Clinical Trials: A Practical Guide for Research Compliance, is an understandable, easy-to-read resource that describes the HIPAA privacy regulations as they apply to research, and how they relate to regulations already in place. HIPAA in Clinical Trials brings together all the HIPAA regulations relating to research, making it a tool you can use to maintain compliance in a wide variety of research situations.
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Whether you're new to HIPAA or looking to take your knowledge to the next level, HIPAA in Clinical Trials: A Practical Guide for Research Compliance will help you:
- Understand what HIPAA means for clinical trials through clear, plain-English interpretations of the regulation.
- Achieve compliance through use of case scenarios.
- Create customized policies and procedures for your research facility quickly by downloading and modifying samples on the CD-ROM.
- Manage difficult research situations that have been impacted by HIPAA, such as dealing with operations staff.
- Grasp research-specific HIPAA topics such as authorizations, pre-screening processes, and de-identified information.
- Navigate the areas of HIPAA that have been "hanging up" researchers.
HIPAA in Clinical Trials: A Practical Guide for Research Compliance is the first and only book and CD-ROM resource on this topic. Whether your research is done at a hospital, clinic, or contract research organization (CRO), HIPAA in Clinical Trials will give you the expert analysis of the regulation you need to ensure HIPAA compliance. Order your copy today!
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