FDA-HUMAN PHARMACEUT › Providing Regulatory Submissions in Electronic Format - Certain Human Pharmaceutical Product Applications and Related Submissions Using the eCTD Specifications - Guidance for Industry
Providing Regulatory Submissions in Electronic Format - Certain Human Pharmaceutical Product Applications and Related Submissions Using the eCTD Specifications - Guidance for Industry
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Document Number
FDA-HUMAN PHARMACEUT
Revision Level
REVISION 3
Status
Current
Publication Date
May 1, 2015
Page Count
15 pages