The 2013 CFR/ICH GCP Reference Guide contains:
- Updated as of April 1, 2013! FDA Code of Federal Regulations, Good Clinical Practice Parts 11, 50, 54, 56, 312, & 314.
- ICH Guidelines Good Clinical Practice (E6) and Clinical Safety Data Management (E2A).
- The European Union Clinical Trials Directive and The European Union Good Clinical Practice Directive.
The convenient and easy-to-reference pocket guide is ideal for new hire packets, giveaways, IRBs, regulatory personnel, QA/QC departments, institutions, site and management organizations, CRAs, sponsors, investigator meetings, research facilities, universities, hospitals, and more! The CFR/ICH Reference Guide provides the critical information you need to know to stay current with the industry’s codes and regulations. Custom Covers and Multiple Copy Discounts Available! Call: 1-800-856-2556 | Email: email@example.com Standard orders of 100+ books are only $9.95 per book! This Guide can also be customized with your company logo for orders of 100+ books. Call for details.
4'x7' spiral bound soft cover pocket guide.
Spiral binding also available.
Device-Specific CFR Guide also available.