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Table of Contents
1 Clinical Trials: Historical Aspects and Importance and New Drug Developments
2 The Definition of GCP
3 The Principles of GCP
4 The Drug Development Process and Evolution of Regulations
5 Planning Clinical Research
6 Preparation of Ethics Committee (IRB) Proposal
7 Preparation of Informed Consent
8 Preparation of Findings Tables
9 Setting the Ideal Statistical Methods
10 The Duties of a Clinical Research Coordinator
11 The Duties of Clinical Researchers
12 The Phases of Clinical Studies
13 Safety in Clinical Trials
14 Setting the Size
15 Setting the Ideal Method
16 Ethics of Clinical Research
17 Recruitment and Enrolment
18 Why we need Clinical Consent and Other Documentation
19 Monitoring the Trial
20 Inspection
21 Ethics
Institutional Review Board/Independent Ethics Committee(IRB/IEC)
22 Responsibilities of the Investigator
23 Responsibilities of the Sponsor
24.Clinical Trial Protocols.
2 The Definition of GCP
3 The Principles of GCP
4 The Drug Development Process and Evolution of Regulations
5 Planning Clinical Research
6 Preparation of Ethics Committee (IRB) Proposal
7 Preparation of Informed Consent
8 Preparation of Findings Tables
9 Setting the Ideal Statistical Methods
10 The Duties of a Clinical Research Coordinator
11 The Duties of Clinical Researchers
12 The Phases of Clinical Studies
13 Safety in Clinical Trials
14 Setting the Size
15 Setting the Ideal Method
16 Ethics of Clinical Research
17 Recruitment and Enrolment
18 Why we need Clinical Consent and Other Documentation
19 Monitoring the Trial
20 Inspection
21 Ethics
Institutional Review Board/Independent Ethics Committee(IRB/IEC)
22 Responsibilities of the Investigator
23 Responsibilities of the Sponsor
24.Clinical Trial Protocols.