Clinical data management

Results: 1569



#Item
761Pharmaceutics / Food and Drug Administration / Pharmaceutical sciences / Clinical Data Management / Pharmaceuticals policy / Title 21 CFR Part 11 / Clinical trial / Validation / Audit trail / Clinical research / Pharmaceutical industry / Research

Guidance for Industry COMPUTERIZED SYSTEMS USED IN CLINICAL TRIALS U.S. Department of Health and Human Services Food and Drug Administration

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Source URL: www.fda.gov.

Language: English
762Clinical Data Management / Electronic Common Technical Document / Recruitment / Management / Validation / Electronic submission / Human resource management / Cover letter / Clinical research / Research / Pharmaceutical industry

MEMBER STATES RECOMMENDATION ON THE COVER LETTER FOR NEW APPLICATIONS SUBMITTED THROUGH THE MRP/DCP Doc. Ref.: CMDh[removed]Rev3 March[removed]With every MA application, the applicant is required to provide a cover letter

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Source URL: www.hma.eu

Language: English - Date: 2012-03-27 09:26:07
763Patient-reported outcome / Disability / Mpro / Education / Science / Academia / Clinical Data Management / Clinical research / Comorbidity

The link between frailty, disability and polypathology Figure 1: Definitions of frailty, comorbidities (polypathology) and disability, and their major healthcare implications in the general population.1 Reproduced with p

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Source URL: myhivclinic.org

Language: English - Date: 2013-04-23 14:29:56
764Research / Drug safety / Medical informatics / Clinical research / Clinical Data Management / Vaccine Adverse Event Reporting System / Structured Product Labeling / Electronic Common Technical Document / Adverse Event Reporting System / Medicine / Food and Drug Administration / Health

FDA Regional Technical Specifications for ICH E2B (R3) Implementation Postmarket Submission of Individual Case Safety Reports (ICSRs) for Vaccines Draft Technical Specifications Document This Document is incorporated by

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Source URL: www.fda.gov

Language: English
765Aall / Evaluation / Clinical Data Management / Clinical research / Electronic patient-reported outcome

AALL Excellence in Marketing Award Entry Form Instructions Please review the Award Guidelines. Be certain the material or activity fits one of the entry categories established. When answering questions below, specify how

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Source URL: www.aallnet.org

Language: English
766Pharmaceutical industry / Electronic Common Technical Document / Grants / Electronic submission / Validation / Science / Medicine / Clinical research / Research / Clinical Data Management

MEMBER STATES RECOMMENDATION ON THE COVER LETTER FOR NEW APPLICATIONS SUBMITTED THROUGH THE MRP/DCP Doc. Ref.: CMDh[removed]Rev2 April 2008Rev3 March 2012

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Source URL: www.hma.eu

Language: English - Date: 2012-03-27 09:26:08
767Medical informatics / Medicine / Electronic Common Technical Document / Pharmaceutical industry / Drug safety / Food and Drug Administration / Validation / Bookmark / Investigational New Drug / Clinical research / Research / Clinical Data Management

Microsoft PowerPoint[removed]Ventura.ppt

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Source URL: www.fda.gov

Language: English
768Medical informatics / Electronic health record / Medicare / Practice management software / Health / Health informatics / Medicine

QUALIFIED CLINICAL DATA REGISTRY CRITERIA FOR SUBMISSION OF 2014 PHYSICIAN QUALITY REPORTING SYSTEM (PQRS) DATA

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Source URL: www.cms.gov

Language: English - Date: 2014-08-21 14:12:35
769Clinical research / Pharmacology / Food and Drug Administration / Clinical Data Management / Medical informatics / Clinical Data Interchange Standards Consortium / Microsoft PowerPoint / Center for Drug Evaluation and Research / Electronic Common Technical Document / Pharmaceutical sciences / Research / Medicine

Computational Science and Data Standards in CDER ` Chuck Cooper, M.D.

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Source URL: www.fda.gov

Language: English
770Medical informatics / Competitions / Digital media / Research / Electronic Common Technical Document / Science / Electronic submission / Graphical user interface / Portable Document Format / Computing / Clinical Data Management / Clinical research

Ensuring a Successful Submission Connie Robinson-Kuiperi, RAC, PMP Office of Business Process Support Center for Drug Evaluation and Research November 5, 2008

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Source URL: www.fda.gov

Language: English
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