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LEADER 02017nam 2200433Ia 4500

001 ocn369245702;

003 OCoLC;

005 20141212041353.0;

006 m d f ;

007 cr an|||||||||;

008 090603s2007 mdu s f000 0 eng d;

035 a| (Sirsi) o369245702;

035 a| (OCoLC)369245702;

040 a| GPOc| GPOd| UtOrBLW;

049 a| ERE#;

074 a| 0499-T (online);

086 0 a| HE 20.4702:R 26/5;

245 00 a| Guidance for industry :b| providing regulatory submissions in electronic format, receipt date.;

246 30 a| Providing regulatory submissions in electronic format, receipt date;

260 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| [2007];

300 a| 6 pages :b| digital, PDF file.;

336 a| text2| rdacontent;

337 a| computer2| rdamedia;

338 a| online resource2| rdacarrier;

500 a| Title from PDF title page (viewed on June 3, 2009).;

500 a| "Draft guidance".;

500 a| "June 2007".;

538 a| Mode of access: Internet at the FDA web site. Address as of 6/3/09: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM072385.pdf ; current access is available via PURL.;

650 0 a| Electronic filing systemsx| Government policyz| United States.=| ^A827407;

710 2 a| Center for Drug Evaluation and Research (U.S.)=| ^A431016;

710 2 a| Center for Biologics Evaluation and Research (U.S.)=| ^A368272;

856 40 u| https://purl.fdlp.gov/GPO/LPS113402;

949 a| Click on web addressw| ASISh| JOYNER94o| jlhb;

998 a| 1900162;

998 a| u1900162;

596 a| 1;

999 a| CLICK ON WEB ADDRESSw| ASISc| 1i| 1900162-1001l| JNETm| JOYNERr| Ys| Yt| JNE1DOu| 9/16/2009x| EDOCUMENTz| JERESOURCEo| .STAFF. jlhb;

Guidance for industry : providing regulatory submissions in electronic format, receipt date.

Other author	Center for Drug Evaluation and Research (U.S.)
Other author	Center for Biologics Evaluation and Research (U.S.)
Format	Electronic
Publication Info	Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [2007]
Description	6 pages : digital, PDF file.
Supplemental Content	https://purl.fdlp.gov/GPO/LPS113402
Subjects	Electronic filing systems--Government policy. --United States. Drugs--Testing. --Government policy. --United States. Biologicals--Evaluation. --Government policy. --United States.

Portion of title	Providing regulatory submissions in electronic format, receipt date
General note	Title from PDF title page (viewed on June 3, 2009).
General note	"Draft guidance".
General note	"June 2007".
Technical details	Mode of access: Internet at the FDA web site. Address as of 6/3/09: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM072385.pdf ; current access is available via PURL.
GPO item number	0499-T (online)
Govt. docs number	HE 20.4702:R 26/5

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Guidance for industry : providing regulatory submissions in electronic format, receipt date.

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