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Electronic common technical document
Results: 446

#	Item
351	Submitting High Quality eCTD Submissions to FDA/OGD Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Medical informatics Electronic Common Technical Document Digital media Common Technical Document Food and Drug Administration Electronic submission Publishing Filing Clinical Data Management Clinical research Research
352	Microsoft PowerPoint - CDER eCTD and Validation Update.ppt [Compatibility Mode] Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Medical informatics Clinical Data Management Pharmaceutical industry Electronic Common Technical Document Center for Drug Evaluation and Research Validation Abbreviated New Drug Application Clinical research Research Pharmaceutical sciences
353	Microsoft PowerPoint - Plenary Session 3 - Robinson - Module-1-Presentation v4.ppt [Compatibility Mode] Add to Reading List Source URL: www.fda.gov Language: English Software Computing Electronic Common Technical Document Competitions Digital media Research Microsoft PowerPoint HTML element Electronic submission Clinical Data Management Clinical research Medical informatics
354	Microsoft PowerPoint - San Diego Tutorial.ppt Add to Reading List Source URL: www.fda.gov Language: English Medicine Medical informatics Electronic Common Technical Document Pharmacology Common Technical Document Food and Drug Administration Clinical trial Regulated Product Submissions Clinical Data Management Research Clinical research
355	Microsoft PowerPoint - STF-final [Compatibility Mode] Add to Reading List Source URL: www.fda.gov Language: English Clinical Data Management Electronic Common Technical Document HTML element Food and Drug Administration Clinical research Research Pharmaceutical sciences
356	Microsoft PowerPoint - GPHA-Reviewable-ANDA.ppt Add to Reading List Source URL: www.fda.gov Language: English Medical informatics Medicine Electronic Common Technical Document Pharmaceutical industry Quality Food and Drug Administration Validation Clinical research Research Clinical Data Management
357	eCTD Post Approval CMC Aspects: FDA Perspective Hasmukh B. Patel, Ph.D. ONDQA, CDER, FDA AAPS Workshop Baltimore, Maryland Add to Reading List Source URL: www.fda.gov Language: English Clinical Data Management Medical informatics Electronic Common Technical Document Pharmacology Drug safety Food and Drug Administration Research Clinical research Medicine
358	Microsoft PowerPoint[removed]Gensinger.ppt Add to Reading List Source URL: www.fda.gov Language: English Research Clinical research Food and Drug Administration Clinical Data Management Standards organizations Clinical Data Interchange Standards Consortium Prescription Drug User Fee Act Structured Product Labeling Electronic Common Technical Document Medical informatics Health Medicine
359	Hussong Slides DIA Annual Meeting 2012 Add to Reading List Source URL: www.fda.gov Language: English Clinical research Drug safety Health Clinical Data Management Medical informatics Electronic Common Technical Document Investigational New Drug New Drug Application Center for Drug Evaluation and Research Food and Drug Administration Research Medicine
360	Microsoft PowerPoint - gensingerg_2.ppt [Compatibility Mode] Add to Reading List Source URL: www.fda.gov Language: English Medical informatics Pharmaceutical industry Electronic Common Technical Document Validation Medicine Clinical research Research Clinical Data Management

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