4.5
428
ratings

Course Currilcum
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- CDM Materials and Notes Unlimited
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- Clinical trail Process.mp4 01:47:00
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- Clinical trail Process.mp4 01:06:00
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- Phases of Clinical trial Process.mp4 00:59:00
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- CRF Contents.mp4 01:00:00
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- CRF VS ECRF Contents.mp4 02:02:00
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- What is protocol.mp4 00:56:00
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- Protocol-Safety easement.mp4 01:03:00
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- Protocol-Premature withdrawal and unscheduled visits.mp4 00:20:00
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- Protocol-datamonitoring.mp4 00:35:00
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- Data coding 00:57:00
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- ICH GCP guidelines.mp4 00:50:00
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- CDM Process.mp4 01:03:00
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- Role of CDM in Clinical trails.mp4 01:03:00
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- Study start-up in Clinical trails.mp4 00:52:00
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- Data Collection Methods.mp4 00:51:00
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- Data Entry and validation.mp4 00:58:00
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- Univariate Vs Multivariate.mp4 01:22:00
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- Database Lock and Freez.mp4 00:59:00
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- Introduction to Oracle clinical and different windows.mp4 00:56:00
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- Role of Clinical trial gov website in Clinical trails.mp4 00:19:00
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- Study Start-up and Study design with OC.mp4 00:55:00
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- Creating Intervals and Events with OC.mp4 01:00:00
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- AE,SAE&reconciliation.mp4 02:03:00
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- CRF design with OC Questions.mp4 01:52:00
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- Question Groups.mp4 01:03:00
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- DCM, DCI Creation.mp4 00:58:00
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- ECRF.mp4 00:59:00
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- ECDIT Checks.mp4 02:01:00
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- Data discrepancy management.mp4 01:14:00
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- Database Lock and freeze Detailed.mp4 00:55:00
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- DMP and CCG.mp4 00:54:00
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- EDC.mp4 01:02:00
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- Creating Subjects.mp4 00:51:00
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- Medidatrave walk through.mp4 00:49:00
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- Medidatrave walk through- Labs.mp4 02:36:00
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- Clinical data manger role.mp4 01:09:00