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Title 21 CFRs

Two-Volume Devices/Diagnostics Title 21 CFR Set

April 2013

The federal government has just compiled the new devices/diagnostics-related Title 21 CFR volumes for 2013 with all of the FDA rules for devices updated through April 1, 2013.

Update your library with the latest additions and revisions to the CFR governing quality systems for medical devices and equipment/software manufacturers, Part 11 electronic records and signatures, device enforcement policies, protection of human subjects, good laboratory practices, labeling, medical device reporting, investigational device exemptions, device tracking requirements, postmarket surveillance and more.

Your Two-Volume Title 21 CFR Devices/Diagnostics Set includes:

  • Parts 1–99 (FDA, General)
  • Parts 800–1299 (FDA, Medical Devices)

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To order individual copies of the CFRs, click here.