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Roles and Responsibilities in Clinical Trials of Investigator, Study Coordinator, Sponsor, Monitor, ...
Assignment on Experimental Study- RCT and Non RCT, Observation Study: Cohort, Case Control, Cross se...
Pepgra Healthcare is a leading Contract Research Organization (CRO) assisting pharmaceutical, biotec...
Clinical trials are divided in to different phases –Phase 1, Phase 2 and Phase 3 each of which has...
An overview of ICH-GCP guidelines of clinical trials. Good clinical practice (GCP): a standard for t...
The term ‘’essential documents’’ refers to the documents which, according to the ICH-GCP Gui...
Clinical trials are fundamental to the development and approval of new drugs, ensuring their safety,...
Phase-by-Phase Clinical Trial Costs explained with detailed insights on budgeting, patient expenses,...
A clinical trial is a culmination of the several stages of a drug or medical device development prog...
Artificial intelligence is being embedded in the clinical trials field in a way that can benefit the...
here are the clinical research terminologys
Explaining Roles and responsibilities of clinical trial personnel :Investigator,study coordinator,sp...
Investigator roles
Presentation providing brief description of clinical trials, their phases, types, Protocol, developm...
the clinical research team and their Roles & responsibility.
describe about role of sponsor and CRO on clinical trial process
The mission of the Clinical Trials Registry-India (CTRI) is to ensure that all clinical trials condu...
This document describes the detailed information of clinical trial protocol and protocol design. The...
Good clinical practice ICH GCP E6
Clinical research associate responsebility
DEVELOPING CLINICAL TRIAL PROTOCOL
A clinical trial protocol is a comprehensive document that outlines the objectives, design, methodol...
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
