Talk:Outline of clinical research

List updater
In subsection A below, listed are articles which are missing from the List of clinical research topics. They were found by looking in the categories in subsection C. One can add more categories to be searched to subsection C, see some suggestions in subsection D.

All this process can be restarted by clicking on the link at the bottom of subsection E.

Please note that anything around here is editable, but please don't modify the lines of the form

or their order.

A: Articles missing from the List of clinical research topics
Accelrys -- BioPharm (US company) -- CERF Collaborative Framework -- ClearTrial -- ClinLife -- Clinical Data Interchange Standards Consortium -- Clinical data acquisition -- Clinical data management -- Clinical trial management system -- Data monitoring committee -- EClinical trial technology -- Electronic common technical document -- Electronic patient-reported outcome -- EudraCT -- G-DOC -- Information Services Division -- Remote data capture -- Remote data entry -- Scottish Intercollegiate Guidelines Network -- Validation (drug manufacture) -- ALMANAC -- ASTEROID trial -- AURORA trial -- Abdullahi v. Pfizer, Inc. -- Age-Related Eye Disease Study -- Analysis of clinical trials -- Assay sensitivity -- Biological plausibility -- CDR computerized assessment system -- CapOpus -- Cardiac Arrhythmia Suppression Trial -- Clinical trial effect -- Clinical trials on Ayurvedic drugs -- ClinicalTrials.gov -- Confirmatory trial -- Dose-ranging study -- Dublin Molecular Medicine Centre -- European Forum for Good Clinical Practice -- German Acupuncture Trials -- Guatemala syphilis experiment -- H5N1 clinical trials -- IFPMA Clinical Trials Portal -- INIT II -- Imaging biomarker -- Interim analysis -- Jadad scale -- Jesse Gelsinger -- Length time bias -- List of Centers and Institutes at the Perelman School of Medicine -- MIDAS Trial -- Medical experimentation in Africa -- N of 1 trial -- Natural history group -- Patient recruitment -- Potentially all pairwise rankings of all possible alternatives -- Rule of three (medicine) -- Scandinavian Simvastatin Survival Study -- Site management organization -- Standard for Exchange of Non-clinical Data -- Stratify (clinical trials) -- Trial master file -- Trials (journal) -- Tuskegee syphilis experiment -- Women's Health Initiative -- Active placebo -- Clinical Trials Directive -- Clinical endpoint -- Clinical trial portal -- Clinical trials registry -- Cluster randomised controlled trial -- Community advisory board -- Community-based clinical trial -- Consecutive case series -- Contract research organization -- Covered clinical study -- Discovery and development of thalidomide and its analogs -- Drug Efficacy Study Implementation -- Drug design -- ERT (company) -- EUDRANET -- EarlySense -- Ethics committee (European Union) -- EudraGMP -- EudraLex -- EudraPharm -- European and Developing Countries Clinical Trials Partnership -- Eurotrials Scientific Consultants -- Evidence-based design -- Good Clinical Practice -- Good Clinical Practice Directive -- Gustav III of Sweden's coffee experiment -- Haybittle–Peto boundary -- Health Science Scotland -- Health services research -- Hit selection -- Human subject research -- Informed assent -- Institute for OneWorld Health -- Levels of evidence -- List of contract research organizations -- Lost to follow-up -- Monitoring in clinical trials -- Motherisk -- National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research -- Nocebo -- Office for Human Research Protections -- Pearl Index -- Phases of clinical research -- Placebo in history -- Placebo-controlled study -- Pocock boundary -- Population study -- Postmarketing surveillance -- Principal investigator -- Privacy for research participants -- Project SHAD -- Qualified person (European Union) -- Resentful demoralization -- Response-rate ratio -- Sham surgery -- Standard operating procedure -- Therapeutic misconception -- Zelen's design --

B: Place here articles not wanted either in the List of clinical research topics or in subsection A.
Pharmaceutical industry -- Pharmaceutical industry in Bangladesh -- Pharmaceuticals in India --

C: Categories to be searched
The bot will look for potential additions to the List of clinical research topics in this list of categories. You may add any other categories to this list, for example from subsection D below. Use the format Category:XXX (the colon shows up twice!).

Category:Clinical data management -- Category:Clinical trials -- Category:Clinical research

D: Potential searchable categories
Move up to subsection C any categories which the bot should search for missing articles in the List of clinical research topics.

Category:Clinical trial organizations -- Category:Clinical trials related to HIV -- Category:Clinical pharmacology -- Category:Clinical research ethics -- Category:Contract research organizations -- Category:Drug discovery -- Category:Experimental medical treatments -- Category:Good Clinical Practice -- Category:Meta-analysis -- Category:National agencies for drug regulation -- Category:Systematic review -- Category:Therapeutics --

E: Articles in List of clinical research topics not in categories
May be redirects or articles which should be removed/categorized.

Office of Regulatory Affairs -- Investigational product -- Active ingredient -- MedWatch -- Commissioner of Food and Drugs -- U.S. Food and Drug Administration -- FDA Fast Track Development Program -- Prescription Drug User Fee Act -- Medical device -- Cohort study -- Biopharmacology -- Framingham Heart Study -- COSTART -- Prescription drug -- Directive 95/46/EC on the protection of personal data -- Hazard ratio -- Systematic review -- Standing operating procedure -- Longitudinal study -- Clinical Trial Management System -- Abbreviated New Drug Application -- Biopharmaceutical -- Ethics Committee (European Union) -- Quintiles -- JANUS clinical trial data repository -- Pharmacokinetics -- Biotechnology -- Epidemiology -- Pharmacology -- Norwegian Medicines Agency -- Adverse drug reaction -- PharPoint Research -- Systematized Nomenclature of Medicine -- Clinical monitoring -- Orphan disease -- Off-label use -- Relative risk -- Number needed to treat -- Health Insurance Portability and Accountability Act -- Multicenter AIDS Cohort Study -- Clinical trial protocol -- Therapeutic Goods Administration -- Seeding trial -- Medical writing -- Cross-sectional study -- Medicinal product -- Institutional review board -- Informed consent -- Covance -- Data monitoring committees -- Strengthening the reporting of observational studies in epidemiology -- Epidemiological methods -- Electronic Common Technical Document -- Clinic -- Australian Drug Evaluation Committee -- Regulatory requirement -- Subgroup analysis -- Center for Drug Evaluation and Research -- Good clinical practice -- Case-control study -- Retrospective cohort study -- Biomedical research -- Number needed to harm -- State Food and Drug Administration -- Vaccine -- Tuskegee Study of Untreated Syphilis in the Negro Male -- Substantial equivalence -- Clinical pharmacology -- Title 21 of the Code of Federal Regulations -- Case report -- Pharmacodynamics -- Uppsala Monitoring Centre -- Orphan drug -- Clinical data repository -- Odds ratio -- Case series -- Excipient -- Therapeutic effect -- Case study -- Sensitivity and specificity -- Risk-benefit analysis -- Drug -- Investigational New Drug -- Food and Drugs Act -- Pharmacovigilance -- Remote Data Entry -- Therapeutic Products Directorate -- Federal Food, Drug, and Cosmetic Act -- Observational study -- Directive 2005/28/EC -- MedDRA -- Center for Biologics Evaluation and Research -- Directive 2001/20/EC -- Preclinical -- Great ape research ban -- List of biotechnology articles -- Center for Devices and Radiological Health -- Nested case-control study -- Pharmacometrics -- WHOART -- Prospective cohort study -- Placebo-controlled studies -- Standard for Exchange of Non-clinical Data (SEND) -- Westat -- Suspected Adverse Reaction Surveillance Scheme -- Swedish Medical Products Agency -- Parexel -- Meta-analysis -- Clinical site --

Refresh the above lists

Very important article
This is very important article. --Abhijeet Safai (talk) 06:22, 18 October 2014 (UTC)

Quick explanation of Wikipedia outlines
"Outline" is short for "hierarchical outline". There are two types of outlines: sentence outlines (like those you made in school to plan a paper), and topic outlines (like the topical synopses that professors hand out at the beginning of a college course). Outlines on Wikipedia are primarily topic outlines that serve 2 main purposes: they provide taxonomical classification of subjects showing what topics belong to a subject and how they are related to each other (via their placement in the tree structure), and as subject-based tables of contents linked to topics in the encyclopedia. The hierarchy is maintained through the use of heading levels and indented bullets. See Outlines for a more in-depth explanation. The Transhumanist 00:04, 9 August 2015 (UTC)