Course fee $275 per participant

The course is offered by Research Support Centre (RSC), a centre with renowned history of delivering high quality training courses and services in clinical trial monitoring, Data Management and communication. RSC’s courses are delivered by highly qualified facilitators, guaranteeing the trainees of invaluable training standards.
Target Audience: Investigators, Clinical Trial Managers & Coordinators, Study Clinicians, Medical Doctors, Clinical Officers, Medical Assistants, Research Nurses, Laboratory Technicians, Laboratory Assistants, Data Managers, Data Officers, Trial Coordinators, Field Officers and all interested Health Professionals.
Pre-requisite: clinical research experience
Application deadline: Applications should be submitted to rsccourses@medcol.mw(with a copy to rscinformationunit@gmail.com) no later than Monday, 16th January, 2017.
About the course: This course will cover 12 modules and an assessment.

• Phases of Clinical Research
• Key Players in Clinical Trials,
• Principles of Good Clinical Practice (GCP)
• Clinical Research Protocol,
• Informed Consent Process,
• Ethics Committees and Regulatory Authorities,
• Managing Investigational Product
• Adverse Events – Safety Reporting,
• Principles of Documentation,
• Monitoring, Audits and Inspections,
• Quality control and Quality Assurance
• Site preparation and Management

Course fees cover course material, lunch and refreshments.
If you need more information, send an email to info@medcol.mw (with a copy torscinformationunit@gmail.com) or call on +265 (0) 888 366 394/ +265 (0)993 137 527.