Clinical Trial Source Data Verification
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Clinical Trial Source Data Verification
6:40
Unauthorised herpes vaccine clinical trial GCP case study
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Unauthorised herpes vaccine clinical trial GCP case study
15:43
Clinical Trial Source data introduction
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Clinical Trial Source data introduction
7:25
Clinical research GCP misconduct-case study
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Clinical research GCP misconduct-case study
8:55
GCP deviations at monitoring visit-case study
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GCP deviations at monitoring visit-case study
4:22
Clinical Trial Drug Return and Destruction
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Clinical Trial Drug Return and Destruction
5:51
Clinical Trial Drug Compliance
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Clinical Trial Drug Compliance
6:00
IWRS drug dispensation for clinical trials
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IWRS drug dispensation for clinical trials
7:29
GCP violation-fake medical history
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GCP violation-fake medical history
4:22
GCP violation-investigator misconduct
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GCP violation-investigator misconduct
8:55
Clinical Trial delegation log site coordinator tasks
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Clinical Trial delegation log site coordinator tasks
8:56
Clinical Trial Delegation log part2 PI and SI task
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Clinical Trial Delegation log part2 PI and SI task
7:05
Clinical Trial-Principal Investigator delegation as per GCP
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Clinical Trial-Principal Investigator delegation as per GCP
6:01
Clinical Trial Drug Accountability as per GCP
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Clinical Trial Drug Accountability as per GCP
8:10
1937 Elixir Sulfanilamide Incident
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1937 Elixir Sulfanilamide Incident
3:34
Clinical Trial Protocol Schedule-end of treatment
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Clinical Trial Protocol Schedule-end of treatment
6:15
Clinical Trial Protocol schedule-screening
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Clinical Trial Protocol schedule-screening
7:34
Clinical Trial Protocol schedule-randomization
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Clinical Trial Protocol schedule-randomization
4:30
Clinical Trial Objectives and Endpoints
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Clinical Trial Objectives and Endpoints
8:12
Clinical Trial eligibility criteria
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Clinical Trial eligibility criteria
11:52
Clinical Trials Protocol as per GCP
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Clinical Trials Protocol as per GCP
5:08
Clinical Trial Drug Regulatory Authority-FDA EMA TGA Intro
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Clinical Trial Drug Regulatory Authority-FDA EMA TGA Intro
5:12
IRB/IEC operation as per GCP in Clinical Trials
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IRB/IEC operation as per GCP in Clinical Trials
7:43
IRB/IEC in Clinical Trials-composition and function as per GCP
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IRB/IEC in Clinical Trials-composition and function as per GCP
6:57
FDA EMA TGA Global Drug Regulatory Authorities i
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FDA EMA TGA Global Drug Regulatory Authorities i
6:30
Tuskegee Syphilis Study-GCP violations
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Tuskegee Syphilis Study-GCP violations
4:52
Clinical Trials Phase III
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Clinical Trials Phase III
3:42
Clinical Trials Phase II
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Clinical Trials Phase II
3:14
Clinical Trial Phase 1
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Clinical Trial Phase 1
5:05
Drug discovery and preclinical testing
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Drug discovery and preclinical testing
5:43
Clinical Trial Phases and Hurdles
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Clinical Trial Phases and Hurdles
2:20
Informed consent process for Clinical Trials
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Informed consent process for Clinical Trials
8:34
Historical events in Clinical Trials
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Historical events in Clinical Trials
3:15
Nuremberg Code for Clinical Trials
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Nuremberg Code for Clinical Trials
8:10
ICH-GCP beginning for Clinical Trials
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ICH-GCP beginning for Clinical Trials
6:13
Declaration of Helsinki
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Declaration of Helsinki
7:49
13 Principles of ICH-GCP
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13 Principles of ICH-GCP
10:52
Drug Development Overview
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Drug Development Overview
2:27
Clinical Trial what is randomised double blind
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Clinical Trial what is randomised double blind
7:27
Tuskegee syphilis experiment
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Tuskegee syphilis experiment
9:03
Nuremberg Code
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Nuremberg Code
9:56
Elixir Sulfonilamide incidence in 1937
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Elixir Sulfonilamide incidence in 1937
3:56