Sentence examples for regulatory terminology from inspiring English sources

Based on current regulatory terminology, data could be expressed as the adverseEC10, adverseNOEC, and adverseLOEC (as distinct from biomarkerEC10 or biomarkerNOEC values).

MedDRA®, the Medical Dictionary for Regulatory Activities, terminology is the international medical terminology developed under the auspices of the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH).

This chapter presents the various aspects of medical dictionary for regulatory activities terminology MedDRA®.

To allow comparison between all phenotype databases (pharmacology and genetics), we used the Unified Medical Language System UMLSS) Metathesaurus (2015AB release), the MetaMap natural language processing (NLP) tool (MetaMap2016, r2016-01), and the UMLS-Interface software64 to map phenotypes to the terms found in the Medical Dictionary for Regulatory Activities terminology (MedDRA).

aMedDRA (medical dictionary for regulatory activities) terminology.

All AEs were coded using Medical Dictionary for Regulatory Activities terminology.

AEs were coded using Medical Dictionary for Regulatory Activities terminology.

Adverse events were coded using the Medical Dictionary for Regulatory Activities terminology.

Safety was assessed by recording all TEAEs using the Medical Dictionary for Regulatory Activities terminology, vital signs, 12-lead ECG, clinical laboratory test results and body weight.

Patients' and healthcare professionals' reports are coded according to MedDRA (Medical Dictionary for Regulatory Activities) terminology, individually assessed by trained assessors and stored in the same database.

AEs were coded on the basis of the Medical Dictionary for Regulatory Activities terminology version 6.0 and were graded for severity according to the National Institutes of Health Division of Microbiology and Infectious Diseases Adult Toxicity Tables (Version May 2001).