Clinical research Entrance Exam

The syllabus for ICRI Ph.D. clinical research entrance exam covers the following subjects:Biostatistics: This includes topics such as probability, hypothesis testing, regression analysis, and survival analysis.Research methodology: This includes topics such as study design, data collection, data analysis, and interpretation of results.Clinical research: This includes topics such as drug development, clinical trials, and pharmacovigilance.Ethics in research: This includes topics such as informed consent, confidentiality, and plagiarism.The exam is a multiple-choice exam with 100 questions. Each question has four possible answers, and you have 2 hours to complete the exam. The exam is scored on a scale of 0 to 100, and the minimum passing score is 50.To prepare for the exam, you can use the following resources:ICRI's official website: The website has a study guide and practice tests that you can use to prepare for the exam.Books: There are many books available on biostatistics, research methodology, clinical research, and ethics in research.Online courses: There are many online courses available that can help you prepare for the exam.If you are serious about pursuing a Ph.D. in clinical research, I recommend taking the ICRI Ph.D. clinical research entrance exam. The exam is a good way to assess your knowledge and skills in clinical research, and it can help you get into a top clinical research program.Here are some additional tips for preparing for the exam:Start studying early: The exam is 2 months away, so it is important to start studying early.Create a study schedule: Create a study schedule that works for you and stick to it.Take practice tests: Take practice tests to get used to the format of the exam and to identify your areas of weakness.Get help from a tutor: If you are struggling with a particular subject, consider getting help from a tutor.I hope this helps!

Clinical Research is one of the most knowledge-intensive industry. It is complete biography of drug from its inception in the lab to its introduction to the consumer market and beyond. Any molecule is identified is subjected to pre-clinical and clinical trials before entering in to market. Though postmarketing surveillance is also part of the same.
Pre-clinical studies is associated with effect of drug on animals. All the toxicological studies, tests for teratogenicity, carcinogenicity are carried out.
After this, the data obtained from the studies are submitted as an IND (Investigational Drug Application) to take permission for human studies. Then, it is enter in to clinical trials. There are 4 phases in it.
SCOPE-
It is very clear that India has become a very preferred destination for clinical research. The industry is growing exponentially and is expected to reach Rs. 7000 Cr by 2010. Statics shows that if India's clinical trial business grows to 10% of that in US by 2015, the industry will need approximately 50,000 clinical research professionals.
Any professionals from CRO (Clinical Research Organisation), Pharmaceutical, biotech, practising doctors and fresh graduates can apply for it. Salary states is high. As arond 700 Cr. expanditure is there for single research.
M.Pharm, any branch on your own interest has greater opportunity. Right now Pharmaceutics and pharmacology has greater scope. Also pharmacognosy people as Herbal Industries are booming in India. But choosing branch or subject on your interest is more beneficial as one can give free flow of thoughts and also new innovations. So, demand is there for all branch but only on one condition that you have basic to the latest knowledge.