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:
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
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To order individual copies of the CFRs, click here.
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