The new HIPAA regulations will substantially impact clinical research activity - most notably the informed consent process. This new guidebook from CenterWatch is designed to assist clinical research professionals in complying with the new and final HIPAA regulations.
Ensuring a HIPAA-Compliant Informed Consent Process - both an instruction manual and reference resource -- provides detailed guidelines on how to manage and conduct a HIPAA compliant and IRB-acceptable informed consent process. The guide includes sample language and templates for the HIPAA Authorization Form and informed consent forms for use in a variety of clinical research studies including genetic testing, tissue banking and assent. An extensive glossary of terms for use in preparing informed consent documents and convenient and easy-to-reference regulatory guidelines are also included.
Book features:
- Practical approaches to incorporating HIPAA language into a wide variety of informed consent forms
- Discussion of Common Rule requirements and GCP-ICH recommendations
- Sample HIPAA-compliant language and useful templates
- How to examine whether the consent language puts your institution at risk
- Ways to avoid unnecessary IRB objections
"synopsis" may belong to another edition of this title.
Written by Kimberly Irvine and Eileen Hilton, MD - clinical research professionals with more than 20 years of experience conducting clinical trials and managing and operating IRBs.
"About this title" may belong to another edition of this title.
Seller: World of Books (was SecondSale), Montgomery, IL, U.S.A.
Condition: Good. Item in good condition. Textbooks may not include supplemental items i.e. CDs, access codes etc. Seller Inventory # 00105844242
Seller: Revaluation Books, Exeter, United Kingdom
Paperback. Condition: Brand New. 158 pages. 8.75x6.00x0.50 inches. In Stock. Seller Inventory # 1930624395
Quantity: 1 available