Our 2009 CFR/ICH GCP Reference Guide contains:
- FDA Code of Federal Regulations, Good Clinical Practice parts 11, 50, 54, 56, 312, & 314
- Good Laboratory Practice Part 58
- 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
New Feature for 2009!
"Editor's Notes" that alert you to changes to the Federal Register that will take effect after the April 1, 2009 publication date.
Updated annually in April.
Standard orders of 100+ books are only $7.95 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.