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Dictionary of Pharmaceutical Medicine

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Cover of 'Dictionary of Pharmaceutical Medicine'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 abbreviated new drug application
  3. Altmetric Badge
    Chapter 8 accelerated testing
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    Chapter 10 acceptable quality level (AQL)
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    Chapter 16 active implantable medical device
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    Chapter 20 active substance
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    Chapter 26 addendum
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    Chapter 27 additive effect
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    Chapter 30 administration
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    Chapter 37 adverse event report format
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    Chapter 40 age
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    Chapter 46 allele
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    Chapter 47 allele frequency
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    Chapter 50 allocation
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    Chapter 57 alternative splicing
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    Chapter 66 anecdotal study
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    Chapter 70 antagonism
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    Chapter 76 antisense drug
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    Chapter 86 assay
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    Chapter 90 ATC exemption scheme
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    Chapter 98 autoimmune disease
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    Chapter 100 average
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    Chapter 102 balanced study
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    Chapter 104 bar code
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    Chapter 108 batch number
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    Chapter 121 bioinformatics
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    Chapter 123 biological medicinal products
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    Chapter 125 biological rhythm
  29. Altmetric Badge
    Chapter 127 biopharmaceutical
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    Chapter 142 brand name
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    Chapter 144 Broca-formula
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    Chapter 146 bug log
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    Chapter 155 CAPLA
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    Chapter 157 carcinogen
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    Chapter 159 cardiac index
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    Chapter 161 carrier-based drug delivery
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    Chapter 163 case-fatality rate
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    Chapter 172 cell culture
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    Chapter 174 cell line
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    Chapter 176 censored data
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    Chapter 191 circadian rhythm
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    Chapter 195 clean area
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    Chapter 197 clerical error
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    Chapter 199 clinical hold
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    Chapter 200 clinical investigation
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    Chapter 217 clinical trial manager
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    Chapter 219 clinical trial notification (CTN)
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    Chapter 230 Cockcroft formula
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    Chapter 232 code breaking procedures
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    Chapter 234 codon
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    Chapter 236 coenzyme
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    Chapter 247 community based trials
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    Chapter 251 compassionate investigational new drug
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    Chapter 255 complementary medicine
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    Chapter 262 computer assisted product licensing application review
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    Chapter 264 concertation procedure
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    Chapter 266 concomitant medication
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    Chapter 270 confidence limits
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    Chapter 281 Container closure system
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    Chapter 283 contingency table
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    Chapter 287 contract CRA
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    Chapter 301 correction log
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    Chapter 307 COSTART
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    Chapter 309 cost/consequence analysis (CCA)
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    Chapter 320 cross contamination EC
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    Chapter 324 CTX-scheme
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    Chapter 326 cumulative incidence
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    Chapter 343 data edit form
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    Chapter 354 data and safety monitoring board (DSMB)
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    Chapter 358 data validation
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    Chapter 360 Dear Doctor letter
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    Chapter 362 debriefing meeting
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    Chapter 364 dechallenge
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    Chapter 371 demographic data
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    Chapter 375 development international birth date (DIBD)
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    Chapter 379 diagnosis
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    Chapter 392 direct-to-consumer (DTC)
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    Chapter 398 disease free survival (DFS)
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    Chapter 414 dosing schedule
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    Chapter 416 double data entry
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    Chapter 418 double masked
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    Chapter 431 drug evaluation cost
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    Chapter 433 drug holiday
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    Chapter 439 drug product
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    Chapter 448 Du Bois formula
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    Chapter 452 ECOG performance status
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    Chapter 454 ecological study
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    Chapter 456 ecotoxicity
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    Chapter 461 effectiveness
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    Chapter 465 effect size (SRM)
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    Chapter 467 ejection fraction
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    Chapter 480 empiric recurrence risk
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    Chapter 486 endpoint
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    Chapter 488 enteral administration
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    Chapter 500 escape medication
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    Chapter 502 essential drug list (EDL)
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    Chapter 521 evidence based prescribing
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    Chapter 542 extender analysis
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    Chapter 544 extension protocol
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    Chapter 555 FDA 1572 form
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    Chapter 559 fifteen days report
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    Chapter 570 follow-up protocol
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    Chapter 572 food
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    Chapter 574 Food and Drug Administration (FDA)
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    Chapter 576 formulary
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    Chapter 591 general sale list medicine (GSL)
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    Chapter 595 generic name
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    Chapter 597 genetic engineering
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    Chapter 611 good clinical research practice (GCRP)
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    Chapter 613 good laboratory practice (GLP)
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    Chapter 632 healing
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    Chapter 649 high-tech procedure
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    Chapter 651 Hochberg correction
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    Chapter 653 homocygote
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    Chapter 655 Huriet
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    Chapter 657 Hygiene program
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    Chapter 662 IFAPP
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    Chapter 666 immediate release form (IR)
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    Chapter 681 inclusion criteria
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    Chapter 683 incubation period
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    Chapter 701 institution
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    Chapter 705 integrated report
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    Chapter 724 international prescribing information
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    Chapter 726 interval scale
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    Chapter 743 investigator initiated trial (IIT)
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    Chapter 745 investigator’s meeting
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    Chapter 756 Karch and Lasagna classification
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    Chapter 758 Keith-Wagener classification
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    Chapter 760 key-punch error
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    Chapter 771 La Fontaine stages
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    Chapter 772 Lasagna’s law
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    Chapter 773 last value carried forward (LVCF)
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    Chapter 775 latent period
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    Chapter 777 Lead Ethics Committee
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    Chapter 779 legally acceptable representative
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    Chapter 790 linear correlation coefficient
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    Chapter 792 line extension
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    Chapter 794 listed adverse drug reaction
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    Chapter 798 local delivery
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    Chapter 810 manufacture EC (IV)
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    Chapter 812 marginal costs
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    Chapter 814 marketing application
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    Chapter 818 masking
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    Chapter 831 mean arterial blood pressure (MAP)
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    Chapter 833 Median
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    Chapter 839 medical management
  147. Altmetric Badge
    Chapter 848 mee-too
  148. Altmetric Badge
    Chapter 850 memorandum of understanding (MOU)
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    Chapter 854 Michaelis-Menten kinetics
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    Chapter 856 micronucleus test
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    Chapter 861 minimal inhibitory concentration (MIC)
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    Chapter 863 minimal toxic dose (MTD)
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    Chapter 867 minimum relevant difference (MIREDIF)
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    Chapter 869 Minnesota code
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    Chapter 880 mortality rate
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    Chapter 882 multidose injection
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    Chapter 888 multi-state procedure
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    Chapter 904 network chart
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    Chapter 906 new active substance (NAS)
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    Chapter 925 non-conventional medicine
  161. Altmetric Badge
    Chapter 927 non-experimental trial
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    Chapter 929 non-new molecular entities (non-NME)
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    Chapter 940 notice-of-claimed investigational exemption for a new drug
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    Chapter 942 nuisance variable
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    Chapter 946 numerical pain scale (NPS)
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    Chapter 948 Nutley system glossary
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    Chapter 955 off-label
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    Chapter 957 ointment
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    Chapter 959 oldest old
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    Chapter 961 oncogene
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    Chapter 963 oncology
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    Chapter 970 open study
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    Chapter 972 optical activity
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    Chapter 974 optical mark recognition
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    Chapter 978 original medical record
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    Chapter 993 pairing
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    Chapter 995 parallel design
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    Chapter 999 parametric test
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    Chapter 1000 parent-child/foetus report
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    Chapter 1009 patient entry card
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    Chapter 1013 patient information sheet
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    Chapter 1017 patient package insert (PPI)
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    Chapter 1018 patient product information (PPI)
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    Chapter 1022 Parouzzi principle
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    Chapter 1035 pharmaceutical benefit manager (PBM)
  186. Altmetric Badge
    Chapter 1043 pharmaceutical medicine
  187. Altmetric Badge
    Chapter 1044 pharmaceutical quality assurance
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    Chapter 1048 pharmacogenetics
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    Chapter 1056 pharmacy drug (P)
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    Chapter 1078 poor metaboliser
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    Chapter 1086 post-marketing safety study
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    Chapter 1091 pragmatic analysis
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    Chapter 1095 predicted environmental concentration (PEC)
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    Chapter 1099 preinvestigation visit
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    Chapter 1102 premarketing agreement (PMA)
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    Chapter 1114 presystemic hepatic elimination
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    Chapter 1115 pretreatment phase
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    Chapter 1118 pretrial visit
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    Chapter 1127 probability
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    Chapter 1145 promotional trial
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    Chapter 1149 prospective study
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    Chapter 1157 pyrogenicity test
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    Chapter 1158 qualification
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    Chapter 1171 query resolution
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    Chapter 1175 Q-value
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    Chapter 1183 range
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    Chapter 1188 raw data
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    Chapter 1196 reconciliation
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    Chapter 1203 reference member state
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    Chapter 1207 reference range
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    Chapter 1212 reimbursement
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    Chapter 1220 repeatability
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    Chapter 1224 repeated significance testing
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    Chapter 1228 reprocessing
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    Chapter 1233 research coordinator
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    Chapter 1237 restricted marketing authorization
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    Chapter 1251 routine monitoring visit
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    Chapter 1259 safety update report
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    Chapter 1272 self-inspection
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    Chapter 1276 serious adverse reaction
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    Chapter 1285 significance level
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    Chapter 1289 sign test
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    Chapter 1297 site visit log
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    Chapter 1300 slow release formulation (SR)
  225. Altmetric Badge
    Chapter 1304 source document
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    Chapter 1313 square-root rule
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    Chapter 1325 starting material
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    Chapter 1326 start-up meeting
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    Chapter 1343 study duration
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    Chapter 1351 study supplies
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    Chapter 1352 subacute toxicity
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    Chapter 1356 subject enrolment log
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    Chapter 1360 substance
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    Chapter 1368 surface
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    Chapter 1369 surrogate
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    Chapter 1377 synergism
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    Chapter 1386 test article
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    Chapter 1390 therapeutic index
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    Chapter 1391 therapeutic potential
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    Chapter 1394 time-event schedule
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    Chapter 1395 time trade-off (TTO)
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    Chapter 1399 total organ carbon (TOC)
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    Chapter 1401 toxic dose level (TDL)
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    Chapter 1414 treatment use
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    Chapter 1418 trial management organisation
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    Chapter 1422 turbo-haler
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    Chapter 1423 two-stage design
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    Chapter 1431 unblinded study
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    Chapter 1435 unlisted adverse drug reaction
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    Chapter 1440 valid case analysis (VC-analysis)
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    Chapter 1444 variable
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    Chapter 1448 virus
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    Chapter 1453 voluntary reporting (VR)
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    Chapter 1461 well-being
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    Chapter 1465 white-coat hypertension
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    Chapter 1466 WHO-adverse reaction dictionary (WHO-ARD)
  257. Altmetric Badge
    Chapter 1483 xenogeneic disease
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Title
Dictionary of Pharmaceutical Medicine
Published by
Springer Vienna, March 2010
DOI 10.1007/978-3-211-89836-9
ISBNs
978-3-21-189835-2, 978-3-21-189836-9
Authors

Nahler, Gerhard

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 36 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 36 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 5 14%
Student > Ph. D. Student 4 11%
Professor 3 8%
Other 2 6%
Researcher 2 6%
Other 2 6%
Unknown 18 50%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 5 14%
Engineering 3 8%
Social Sciences 2 6%
Chemistry 2 6%
Biochemistry, Genetics and Molecular Biology 1 3%
Other 4 11%
Unknown 19 53%