Mobile Medical Applications Guidance for Industry and Food and Drug Administration Staff

 
Docket ID: FDA-2011-D-0530
Agency: Food and Drug Administration (FDA)
Parent Agency: Department of Health and Human Services (HHS)
Docket Details open glossary dialog  
Related RINs: None
Related Dockets: FDA-2014-D-0798
Short Title: Mobile Medical Applications Guidance for Industry and Food and Drug Administration Staff
Keyword(s): cdrh, cdrh20119, cber, moblie medical applications
Type: Nonrulemaking
Docket Status: OPEN
Center: CDRH
Docket Item Code: D
 

Primary Documents

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Comment Period Closed
Oct 19, 2011 11:59 PM ET
Notice
Posted: 08/12/2011
ID: FDA-2011-D-0530-0003
Comment Period Closed
Oct 19, 2011 11:59 PM ET
Notice
Posted: 07/21/2011
ID: FDA-2011-D-0530-0001
Comment Period Closed
Notice
Posted: 02/09/2015
ID: FDA-2011-D-0530-0109
Comment Period Closed
Notice
Posted: 09/25/2013
ID: FDA-2011-D-0530-0107

Supporting Documents

 
The contents of the section were withdrawn at the request of the Food and Drug Administration and the Department of Health and Human Services.

Comments

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142
Comments Received*
*This count refers to the total comment/submissions received on this docket, as of 11:59 PM yesterday. Note: Agencies review all submissions, however some agencies may choose to redact, or withhold, certain submissions (or portions thereof) such as those containing private or proprietary information, inappropriate language, or duplicate/near duplicate examples of a mass-mail campaign. This can result in discrepancies between this count and those displayed when conducting searches on the Public Submission document type. For specific information about an agency’s public submission policy, refer to its website or the Federal Register document.