2.44 GB | 27min 25s | mp4 | 1920X1080 | 16:9
Genre:eLearning |Language:English
Files Included :
FileName :1 Drug Discovery and development.mp4 | Size: (43.18 MB)
FileName :2 Introduction to Clinical Trials.mp4 | Size: (64.84 MB)
FileName :3 Types of clinical trial.mp4 | Size: (70.79 MB)
FileName :4 Stages of the Clinical Research Process.mp4 | Size: (41.97 MB)
FileName :5 5 Planning of the Study and Ethics Approval.mp4 | Size: (72.62 MB)
FileName :6 6 ICH GCP Content and overview &objective.mp4 | Size: (127.91 MB)
FileName :7 7 The evolution of Good Clinical Practice.mp4 | Size: (44.81 MB)
FileName :8 8 Historical background.mp4 | Size: (70.38 MB)
FileName :9 9 DECLARATION OF HELSINKI.mp4 | Size: (161.75 MB)
FileName :10 10 General Principles of the Declaration of Helsinki.mp4 | Size: (54.99 MB)
FileName :11 11 TUSKEGEE SYPHILIS STUDY 1932 TO 1972.mp4 | Size: (51.56 MB)
FileName :12 13 Core Principle of ICH guidline.mp4 | Size: (273.21 MB)
FileName :13 14 Key Process in clinical study.mp4 | Size: (361.55 MB)
FileName :14 14 Key Stakeholder in a Clinical Study.mp4 | Size: (402.92 MB)
FileName :15 15 Key differences beetween R2 and R3.mp4 | Size: (201.85 MB)
FileName :16 16 Elements of GCPs.mp4 | Size: (45.34 MB)
FileName :17 17 ICH guidelines 4 main topics (Quality Safety Efficacy and Multidisciplinary.mp4 | Size: (56.09 MB)
FileName :18 18 Key stakeholders in the research process and responsibilities of IRB IEC.mp4 | Size: (93.78 MB)
FileName :19 19 Investigator Roles and responsibilities.mp4 | Size: (37.88 MB)
FileName :20 20 Roles and responsibilities of the sponsor.mp4 | Size: (36.92 MB)
FileName :21 21 Data Governance role and responsibilities.mp4 | Size: (22.32 MB)
FileName :22 20 Investigator brochure and inform consent process.mp4 | Size: (57.13 MB)
FileName :23 23 CLINICAL TRIAL PROTOCOL AND PROTOCOL AMENDMENT(S).mp4 | Size: (84.94 MB)
FileName :24 24 Ethics committee Responsibilities.mp4 | Size: (17.8 MB)]
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