[June 29, 2011]

Research and Markets: 2011 CFR/ICH GCP Reference Guide for Medical Devices

Research and Markets (http://www.researchandmarkets.com/research/6673e0/2011_cfrich_gcp_r) has announced the addition of the "2011 CFR/ICH GCP Reference Guide for Medical Devices" report to their offering.

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 for Devices provides the critical information you need to know to stay current with the medical device and combination product industry's codes and regulations.

The compact nature of the guide offers an easy way to keep key device regulations right at your fingertips and readily available for quick reference.

Regulations Included Are:

• Title 21 - Food and Drugs
• Good Clinical Practice Parts 11, 50, 54, 56
• Medical Devices and Quality Systems (News - Alert) Parts 801, 803, 806, 807, 812, 814, 820, 822
• Product Jurisdiction (Combination Products) Part 3

Plus:

• ICH Guideline
• Good Clinical Practice (E6)
• as adopted by the FDA

For more information visit http://www.researchandmarkets.com/research/6673e0/2011_cfrich_gcp_r

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