Course Curriculum
| Clinical Research Administration Fundamentals | |||
| Module 01: Introduction to Clinical Research Administration | 00:15:00 | ||
| Module 02: Clinical Trial Design and Planning | 00:11:00 | ||
| Module 03: Ethics and Regulatory Compliance | 00:13:00 | ||
| Module 04: Institutional Review Boards (IRBs) and Ethics Committees | 00:10:00 | ||
| Module 05: Data Management and Recordkeeping | 00:12:00 | ||
| Module 06: Safety Reporting and Adverse Events | 00:10:00 | ||
| Module 07: Clinical Trial Monitoring and Auditing | 00:09:00 | ||
| Module 08: Study Site Management and Quality Control | 00:17:00 | ||
| Module 09: Data Analysis and Reporting | 00:09:00 | ||
| Module 10: The Future of Clinical Research | 00:10:00 | ||
Instructors
17 STUDENTS ENROLLED
Food Hygiene
Health & Safety
Safeguarding
First Aid
Business Skills
Personal Development



