Six Months Training
The eligibility for the program is Graduation/Post Graduation in Life Science
Program Objectives
The program would endow an introduction to the area of clinical trials, with more detailed coverage of some of the key issues to be considered in their design, analysis, documentation and interpretation.
Further the course aims to develop:
Program Methodology
The prospective participants may join the program by submitting Application form with the necessary fees and attachments. The methodology for the program delivery would be:
Learning Outcome
After completion of the course the participant would be able to:
The eligibility for the program is Graduation/Post Graduation in Life Science
Program Objectives
The program would endow an introduction to the area of clinical trials, with more detailed coverage of some of the key issues to be considered in their design, analysis, documentation and interpretation.
Further the course aims to develop:
- A theoretical and practical understanding of the issues involved in the design, conduct, analysis and interpretation of randomized controlled trials of health interventions.
- Skills to scrutinize information, to critically analyze and carry out research, and to communicate effectively.
- Describe the uses and applications of the main types of intervention studies: clinical trials and community trials.
- Describe the essential features and stages in the conduct of a clinical trial, and the role of randomization, use of placebo, blinding / masking and intention-to-treat analysis.
- Discuss the ethical issues involved in the conduct of a clinical trial.
Program Methodology
The prospective participants may join the program by submitting Application form with the necessary fees and attachments. The methodology for the program delivery would be:
- Delivery of the lectures by the technically expertise Faculty.
- Guest Faculty from industry and academia would deliver the lectures.
- Along with the theoretical knowledge student would also get a chance to have a practical oriented understanding of the subject e.g. role of computers in Clinical Trials
- E-learning platform via Moodle would also be employed for the classes.
- Students would also be taken for Industrial and Hospitals visits to have an overview of the entire Clinical trial process.
Learning Outcome
After completion of the course the participant would be able to:
- Have better understanding of Good Clinical Practice (GCP) and Standard Operating Procedures for Clinical Research.
- Participate in design, conduct and management of Global Clinical Trials, conducted at multicentric sites in India and Overseas.
For further details and enquiries
BIOINFORMATICS INSTITUTE OF INDIA
C-56A/28, Sector - 62,
Noida - 201301
(INDIA)
Tel : 0120-432080
C-56A/28, Sector - 62,
Noida - 201301
(INDIA)
Tel : 0120-432080
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