A day in the life of a monitor!
When at a site, the monitor will meet with the Study Coordinator, review the hospital medical records, use the internet database or paper to ′monitor′ their data versus their medical records, issue queries, check master files, count tablets or vials, provide the update to the doctor, and so on. When...
Main Author: | Kunal Shah |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2012-01-01
|
Series: | Perspectives in Clinical Research |
Subjects: | |
Online Access: | http://www.picronline.org/article.asp?issn=2229-3485;year=2012;volume=3;issue=1;spage=32;epage=34;aulast=Shah |
Similar Items
-
Clinical research monitoring: scenarios and challenges
by: Gustavo Adolfo Sierra Romero
Published: (2013-01-01) -
Good clinical practice: International quality standard for clinical trials
by: Radulović Siniša S.
Published: (2003-01-01) -
Why are clinical trials necessary in India?
by: Subramani Poongothai, et al.
Published: (2014-01-01) -
Analyzability of newly developed/commercially promoted drugs among young medical and dental doctors
by: Sonu Gupta, et al.
Published: (2021-01-01) -
STORAGE MANAGEMENT OF CLINICAL RESEARCH SUPPLIES OF A PHASE IIB/III, NATIONAL, MULTI-CENTRE, DOUBLE-BLIND AND RANDOMIZED STUDY
by: Luiz Teruo Kawamoto Junior, et al.
Published: (2016-12-01)