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Clinical Trials Course

Clinical Trials Course
flexible workload of 4 to 360h
certificate recognized by MEC

What will I learn?

Enhance your expertise in clinical trials with our comprehensive course tailored for healthcare professionals in India. Gain a deep understanding of ethical considerations, including informed consent (in the Indian context) and data privacy regulations relevant to India, while mastering trial design and protocol development that adheres to Indian guidelines. Acquire insights into the different phases of clinical trials, data collection methodologies suitable for the Indian population, and statistical analysis techniques commonly used in Indian research. Learn to confidently address challenges such as managing adverse events and participant dropouts within the Indian healthcare system. Our concise, high-quality, and practice-oriented modules will equip you with the essential skills needed to excel in clinical research in India.

Elevify advantages

Develop skills

  • Master ethical standards: Ensure informed consent and adhere to Indian data privacy regulations.
  • Design robust trials: Create effective randomised controlled trials suitable for the Indian context.
  • Develop protocols: Craft comprehensive clinical trial protocols in accordance with Indian regulatory guidelines.
  • Analyse data: Utilise statistical techniques and software tools relevant to Indian clinical research.
  • Manage challenges: Address side effects, manage participant attrition, and maintain trial integrity within the Indian healthcare landscape.

Suggested summary

Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.
Workload: between 4 and 360 hours

What our students say

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EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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