Certificate Course in ICHGCP Good Clinical Practice

Files Included :

1 - Introduction Objectives and Scope.mp4 (118.07 MB)
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2 - Principles of ICHGCP.mp4 (66.21 MB)
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3 - Introduction Roles Responsibilities.mp4 (61.18 MB)
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4 - Composition Function and Operations.mp4 (20.28 MB)
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5 - Procedures Records Submission Communication.mp4 (25.77 MB)
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10 - Ending Clinical trial participation Investigational product management.mp4 (34.39 MB)
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11 - Randomization Unblinding and Records.mp4 (27.59 MB)
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6 - Qualifications Training Resources Responsibilities.mp4 (35.46 MB)
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7 - Communication with IRBIEC Protocol compliance.mp4 (22.15 MB)
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8 - Trial terminationsuspension Participant care Safety reporting.mp4 (90.71 MB)
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9 - Informed Consent of Trial participants.mp4 (95.15 MB)
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12 - Introduction.mp4 (48.78 MB)
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13 - Communication with IRBIEC and Regulatory Authority.mp4 (10.39 MB)
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14 - Sponsor oversight.mp4 (17.55 MB)
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15 - Quality management.mp4 (20.44 MB)
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16 - Noncompliance Safety and Reporting.mp4 (23.67 MB)
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17 - Investigational products DataRecords and Reports.mp4 (80.95 MB)
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18 - Introduction General considerations and Content of IB.mp4 (63.84 MB)
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19 - Introduction and Content of Clinical trial protocol.mp4 (119.19 MB)
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20 - Introduction and Management of Essential Records.mp4 (133.81 MB)
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21 - What to do after this training.mp4 (21.49 MB)
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