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Info on IDE Reports Sent to OMB
[46 Words]
12/03/2012
Guidance on Preclinical Info for Cellular and Gene Therapy Products
[99 Words]
11/29/2012
Comments Sought on Biological Product Constituent Materials
[43 Words]
11/29/2012
Panel to Discuss Shortwave Diathermy Device Reclassification
[121 Words]
11/29/2012
FDA Posts Planned CDRH Guidances
[72 Words]
11/26/2012
Risk Communication Advisory Panel to Meet
[86 Words]
11/26/2012
FDA Amends Dates on Device ID System Rule
[162 Words]
11/19/2012
Comments Sought on Custom Device Exemption
[43 Words]
11/19/2012
FDA Publishes Notice of FDA User Fee System Records
[116 Words]
11/14/2012
Info on Rx Drug User Fee Form Sent to OMB
[49 Words]
10/22/2012
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