<--- Back to Details
First PageDocument Content
Standards organizations / Medical classification / Nursing informatics / SNOMED CT / Clinical Data Interchange Standards Consortium / International Health Terminology Standards Development Organisation / SDTM / Unified Medical Language System / Systematized Nomenclature of Medicine / Medicine / Health / Medical informatics
Standards organizations
Medical classification
Nursing informatics
SNOMED CT
Clinical Data Interchange Standards Consortium
International Health Terminology Standards Development Organisation
SDTM
Unified Medical Language System
Systematized Nomenclature of Medicine
Medicine
Health
Medical informatics

amiajnl[removed]11

Add to Reading List

Source URL: jamia.bmj.com

Download Document from Source Website

File Size: 609,42 KB

Share Document on Facebook

Similar Documents

Health informatics / Health / Medical research / Standards organizations / CDISC / Clinical Data Interchange Standards Consortium / Clinical data management / Clinical research / Non-profit technology / SDTM / LOINC / Health Level 7

PDF Document

DocID: 1pWCY - View Document

Geographic information system / SDTM

Department for Environment, Food and Rural Affairs Version 4.0 Document Reference: magi0057v4.doc MAGIC

DocID: 1aMiE - View Document

Statistics / Pharmacology / Clinical trials / Standards organizations / Clinical Data Interchange Standards Consortium / SDTM / MedDRA / Bioequivalence / Standard for Exchange of Non-clinical Data / Clinical research / Research / Food and Drug Administration

CDER / CBER Study Data Standardization Plan Recommendations ABC Pharma Company Study Data Standardization Plan 1. General Sponsor Information

DocID: 1a7qc - View Document

Food and Drug Administration / Pharmacology / Clinical Data Management / Clinical trials / Clinical Data Interchange Standards Consortium / SDTM / SAS / Pharmaceutical industry / Data quality / Statistics / Research / Clinical research

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

DocID: 18mMI - View Document

Food and Drug Administration / Science / Medical informatics / Medical statistics / Clinical Data Interchange Standards Consortium / SDTM / Clinical data acquisition / Electronic Common Technical Document / Clinical trial / Research / Clinical research / Clinical Data Management

Microsoft Word - Basic Policy on e-studysubmit for NDA.docx

DocID: 1855z - View Document