Product Details

Three-Volume Clinical Trials Title 21 CFR Set

Published: April 2013 | Price: $210

The federal government has just compiled the new clinical trial-related Title 21 CFR volumes for 2013 with all of the FDA rules for drugs, devices and biologics revised through April 1, 2013.

Order your set today from FDAnews — you’ll receive each volume within days of its release.

Updated for 2013
Code of Federal Regulations
Three-Volume Clinical Trials Title 21 CFR Set

Now you can update your library with the latest additions and revisions to:

Volume 1: Parts 1-99 — FDA, General (Protection of Human Subjects)
Volume 5: Parts 300-499 — FDA, Drugs for Human Use (INDs — Responsibilities of Sponsors and Investigators)
Volume 8: Parts 800-1299 — FDA, Medical Devices (Investigational Device Exemptions)

The federal government has compiled the new 2013 CFR volumes. They are not published in order, but FDAnews will automatically ship your order within days of each volume's release.

Order today

Four Reasons to Get Your New CFR Set From FDAnews:

Convenience — Order online and you'll receive an immediate confirmation by email
Confidence — Once you place your order, you can rest assured you'll receive the latest CFR you need — without delay — as soon as it is publicly available
Priority Service — Your CFR will be shipped from our warehouse the day it arrives
Help Line — Not sure which CFR you need? Call us toll free at (888) 838-5578

Buy Now!
Order now! You pay just $210 for these 3 volumes. Each volume will be shipped to you as soon as it's released. Please call (888) 838-5578 for individual volume pricing.

Please add $24 shipping and handling per set for orders shipped to the U.S. and Canada, or $105 per set for orders shipped elsewhere (shipping and handling may be subject to change, depending upon the number of volumes the federal government publishes). Virginia residents add 5 percent sales tax.

NOTE: Each volume will be shipped to you as soon as it’s released.

Satisfaction Guaranteed
Your purchase is 100% guaranteed. If for any reason you decide the set is not for you, simply return the undamaged hard copy within 30 days of purchase and you'll receive a full refund (less shipping/handling).

To order individual copies of the CFRs, click here.

Shopping Cart

Your shopping cart is empty

Resource Center

Tenth Annual Medical Device Quality Congress
From Risk Management to Postmarket Surveillance
Come for this valuable opportunity to hear FDA officials discuss regulatory plans and objectives — and ask questions you need answered; learn from device industry experts, consultants and other experts with actionable tips and strategies you can take straight back to the office; and network with other professionals who understand your challenges; share war stories and insights over a drink. Register Today. Read More
Conducting Bulletproof CAPA Investigations — ADVANCED
Understanding Advanced Critical Thinking Skills and Innovative Techniques to Improve the Quality of Investigations and Understanding the Root Cause
The FDA's new enforcement plan makes one thing clear: Developing a successful CAPA program has never been more important. But creating an FDA-proof CAPA isn’t easy. If only you could pick the brain of someone who is coping successfully with CAPA — the best and the brightest, an industry leader who has devised programs, procedures and solutions that have put companies out in front with the FDA. Well, you can. Register today. Read More
Surviving an FDA Inspection
The FDA’s cadre of freshly trained inspectors — many of whom come directly from industry — and increased focus on specialized inspections are making it harder than ever to predict the outcome of your next FDA inspection. Unless, of course, you have Surviving an FDA Inspection at your fingertips. If you could spend less than $400 to get your drug manufacturing facility fully prepared to face a tough inspection by the FDA, would you even hesitate? ... Of course not! Read More