
Guidance for Industry and FDA Staff - Addition of URLs to Electronic Product Labeling
This guidance represents the Food and Drug Administration's (FDA's) current thinking on this topic.
U.S. Department of Health and Human Services
Food and Drug Administration
Center for Devices and Radiological Health
Office of Communications, Education, and Radiation Programs
Division of Mammography Quality and Radiation Programs
Electronic Products Branch
Contains Nonbinding Recommendations
Preface
Public Comment
You may submit written comments and suggestions at any time for Agency consideration to the Division of Dockets Management, Food and Drug Administration, 5630 Fishers Lane, Room 1061, (HFA-305), Rockville, MD, 20852. Submit electronic comments to www.regulations.gov. When submitting comments, please refer to the exact title of this guidance document. Comments may not be acted upon by the Agency until the document is next revised or updated.
full-text
Guidance Documents (Medical Devices and Radiation-Emitting Products) Guidance for Industry and FDA Staff - Addition of URLs to Electronic Product Labeling


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