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Drug Information Journal|December 11, 1986
Statistical analyses of adverse event data from clinical trials. Special emphasis on serious eventsR T O'NeillDrug Information Journal|December 11, 1986
Regulatory overview: protection of human subjects--IRBS and informed consentS L NightingaleDrug Information Journal|December 11, 1986
The interrelationship of sponsors, clinical investigators, and institutional review boardsT J KirschDrug Information Journal|December 11, 1986
Analysis and control of costs associated with answering drug information requestsF F Hermann, L A WankeDrug Information Journal|September 24, 2013
Evaluation of Data Entry Errors and Data Changes to an Electronic Data Capture Clinical Trial DatabaseJules T Mitchel, Yong Joong Kim, Joonhyuk Choi, et al.Drug Information Journal|December 12, 1982
Selection of scientific periodicals to monitor drug safety information using Excerpta Medica and Japicdoc in the post marketing surveillance of drugsT Kitaguchi, T Nojiri, S Suzuki, et al.Drug Information Journal|December 12, 1982
An Asian perspective on drug and related health care informationE W De Maar, N A Kshirsagar, I DarmansjahDrug Information Journal|December 12, 1983
Clinical case report forms design--a key to clinical trial successC L BerndDrug Information Journal|December 12, 1983
A comprehensive on-line collection systemL Kowitt, R L MarlinDrug Information Journal|December 12, 1983
Statistical considerations in the design, analysis, and interpretation of comparative clinical studiesG G Koch, W A SollecitoPageof 7