No abstract available
MeSH terms
-
Adverse Drug Reaction Reporting Systems / standards*
-
Clinical Trials as Topic
-
Documentation / methods
-
Documentation / standards
-
Drug Design
-
Drug Monitoring / methods
-
Drug-Related Side Effects and Adverse Reactions*
-
Humans
-
Pharmacology, Clinical / standards
-
Product Surveillance, Postmarketing / methods*
-
Terminology as Topic