Found 226 presentations matching your search
Investigator roles
study purpose
Good Clinical Practices and Investigator responsibilities
Explaining Roles and responsibilities of clinical trial personnel :Investigator,study coordinator,sp...
Assignment on Experimental Study- RCT and Non RCT, Observation Study: Cohort, Case Control, Cross se...
Roles and Responsibilities in Clinical Trials of Investigator, Study Coordinator, Sponsor, Monitor, ...
This presentation provides an in-depth overview of the roles and responsibilities of various personn...
Introduction Historical background Sections Principles Ethics committee Responsi...
Good Clinical Practice (GCP) guidelines are a set of international ethical and scientific standards ...
stake holders in clinical trail
This presentation is a brief overview of ICH-GCP guidelines. Although ICH-GCP is a very vast topic, ...
Sponsor Responsibilities in clinical research as per ICH GCP E6
Kiran Rajput MSc. Clinical Research 4th Semester
This presentation provides a comprehensive overview of Good Clinical Practice (GCP), an internationa...
Good clinical practice ICH GCP E6
INVESTIGATOR'S BROCHURE as per ICH E6 (ICH GCP)
Schedule y
Guidelines for clinical trials
21 CFR 312 and 314 are two separate, but related, US Food and Drug Administration (FDA) regulations ...
ROLES AND RESPONSIBLITIES OF CLINICAL TRIAL PERSONNEL-INVESTIGATOR
Lets, just get to know more about safety reporting in clinical trails with some terminologies, repor...
investigator purpose of investigator role of investigator in study
ICH E 6 good clinical practice (GCP)
Recent Changes SAE Reporting Timeline (Updated Oct-2016)
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