Basic course of 4 hours free
Completion certificate
AI tutor
Practical activities
Online and lifelong course
What will I learn?
Advance your healthcare career with our Clinical Research Associate Course (Indian Edition), specifically tailored for professionals aspiring to excel in clinical trials within the Indian context. Master the fundamentals of protocol development, risk management, and adherence to Indian regulatory guidelines. Learn effective participant recruitment strategies applicable in India, ensuring data integrity and confidentiality according to Indian standards. Gain expertise in trial reporting and documentation, all delivered through concise, high-quality modules. Join us to enhance your skills and contribute significantly to clinical research in India.
Live mentoring sessions every week
Rely on our team of specialists to assist you weekly
Imagine learning while clearing your doubts with professionals already in the field! At Apoia, this is possible
Access open sessions with various industry professionals
Expand your network
Share experiences with specialists from diverse fields and solve your professional challenges.
Learning outcomes
Enhance the development of the practical skills listed below
Develop clinical trial protocols: Master study design and methodology relevant to the Indian healthcare landscape.
Implement risk management: Identify and mitigate potential trial risks specific to clinical trials conducted in India.
Ensure regulatory compliance: Navigate Indian regulatory submission processes and ethical approvals (e.g., CDSCO guidelines).
Optimise participant recruitment: Utilise effective channels and ethical practices for recruiting participants in the Indian context.
Manage trial data: Secure data integrity and confidentiality according to Indian data protection regulations.