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| 245 |
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|a Guidance for industry :
|b providing regulatory submissions in electronic format, general considerations.
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|a Providing regulatory submissions in electronic format, general considerations
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|a Rockville, MD :
|b U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :
|b Center for Biologics Evaluation and Research,
|c [1999]
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| 300 |
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|a 1 online resource (17 pages)
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|a text
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| 338 |
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|a online resource
|b cr
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|a "IT 2."
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| 500 |
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|a "January 1999."
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| 500 |
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|a Electronic resource.
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|a Electronic filing systems
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|z United States.
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|a Drug approval
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|a Center for Drug Evaluation and Research (U.S.)
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|b College Station
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| 998 |
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