Food and Drug Administration

Results: 36271



#Item
991Careers in Medical and Scientific Writing Laura McCormick, PhD Vice President Associate Practice Leader Tamara Fink, PhD Associate Scientific Director

Careers in Medical and Scientific Writing Laura McCormick, PhD Vice President Associate Practice Leader Tamara Fink, PhD Associate Scientific Director

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Source URL: casemed.case.edu

Language: English - Date: 2012-04-04 14:13:04
992AAFCO Board Meeting Thursday, January 15th, 2015 2:40pm – 4:30pm CST BOD Present: Dan Danielson, Bob Geiger, Doug Lueders, Ken Bowers, Kristen Green, Mark LeBlanc, Ali Kashani, Richard Ten Eyck Absent:

AAFCO Board Meeting Thursday, January 15th, 2015 2:40pm – 4:30pm CST BOD Present: Dan Danielson, Bob Geiger, Doug Lueders, Ken Bowers, Kristen Green, Mark LeBlanc, Ali Kashani, Richard Ten Eyck Absent:

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Source URL: www.aafco.org

Language: English - Date: 2015-01-27 15:11:59
993Final: April 2, 2015  Feed and Feed Ingredient Manufacturing Committee Report/Minutes Wednesday, January 14, 2015 2:30-4:Mid-Year Meeting

Final: April 2, 2015 Feed and Feed Ingredient Manufacturing Committee Report/Minutes Wednesday, January 14, 2015 2:30-4:Mid-Year Meeting

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Source URL: www.aafco.org

Language: English - Date: 2015-04-08 15:32:31
994Current Issues and Outreach Committee Report/Minutes  Tuesday, January 13, 2015 9:00 – 10:15 PM San Antonio, Texas COMMITTEE RECOMMENDATIONS:

Current Issues and Outreach Committee Report/Minutes Tuesday, January 13, 2015 9:00 – 10:15 PM San Antonio, Texas COMMITTEE RECOMMENDATIONS:

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Source URL: www.aafco.org

Language: English - Date: 2015-03-17 11:04:09
995automated, replicable CDISC conversion  Clinical Trial Data: Automated, Replicable CDISC Conversion Synopsis + IND and NDA programs necessitate recurrent submission of clinical trial data to regulatory agencies in specif

automated, replicable CDISC conversion Clinical Trial Data: Automated, Replicable CDISC Conversion Synopsis + IND and NDA programs necessitate recurrent submission of clinical trial data to regulatory agencies in specif

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Source URL: www.tamr.com

Language: English - Date: 2015-02-18 15:13:15
996Medical Devices Workshop Regulatory insights: China, Europe and U.S.A. 23rd of AprilMichelangelo Hotel, Milan, Italy International panel of speakers: Albrecht Poth Scientific Director Medical Device Testing - Eur

Medical Devices Workshop Regulatory insights: China, Europe and U.S.A. 23rd of AprilMichelangelo Hotel, Milan, Italy International panel of speakers: Albrecht Poth Scientific Director Medical Device Testing - Eur

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Source URL: www.eurofins.it

Language: English - Date: 2015-04-07 05:20:09
997Research / Pharmacology / Drug safety / Food and Drug Administration / Pharmaceutical industry / Response Evaluation Criteria in Solid Tumors / Clinical trial / Adverse effect / Methadone / Medicine / Health / Clinical research

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Source URL: ti.ucsf.edu

Language: English - Date: 2012-12-10 18:49:02
998Identifying Adverse Drug Events by Relational Learning David Page V´ıtor Santos Costa  Sriraam Natarajan

Identifying Adverse Drug Events by Relational Learning David Page V´ıtor Santos Costa Sriraam Natarajan

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Source URL: pages.cs.wisc.edu

Language: English - Date: 2012-10-08 12:25:28
999Microsoft Wordpi.doc

Microsoft Wordpi.doc

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Source URL: www.americanbenefitscouncil.org

Language: English - Date: 2014-02-20 18:30:18
1000Pharmacology / Clinical research / Food and Drug Administration / Ketones / Design of experiments / Response Evaluation Criteria in Solid Tumors / Clinical trial / Methadone / Adverse effect / Medicine / Chemistry / Health

80010Option 1: In the Home tab in Word, check the Paragraph Icon: This will show Hidden Text (and paragraph marks) - recommended for Mac users Option 2: 1. In the top left corner of the Word menu bar, click

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Source URL: ti.ucsf.edu

Language: English - Date: 2012-12-10 18:48:32