Tamil Nadu Police Department Interview Questions and Answers

The parent or legal guardian is responsible for obtaining informed consent for subjects aged 2 to 12 years old.

• The parent or legal guardian should be fully informed about the study and its risks and benefits.

• The parent or legal guardian should be given ample time to ask questions and make an informed decision.

• The informed consent process should be documented thoroughly.

• Assent should also be obtained from the child, if possible.

• If the child is unable to provide assent, the par...read more

Clinical research involves studying the safety and effectiveness of medical treatments and interventions on human subjects.

• Designing and implementing clinical trials

• Recruiting and screening potential study participants

• Collecting and analyzing data

• Ensuring compliance with ethical and regulatory guidelines

• Communicating with study sponsors and investigators

• Managing study budgets and timelines

AE stands for Adverse Event, SAE stands for Serious Adverse Event, ADR stands for Adverse Drug Reaction, and SADR stands for Serious Adverse Drug Reaction.

• AE refers to any unfavorable medical occurrence in a patient during or after the use of a drug or medical device.

• SAE refers to an AE that results in death, is life-threatening, requires hospitalization, causes significant disability, or requires intervention to prevent harm.

• ADR refers to any response to a drug that is noxio...read more

SOP stands for Standard Operating Procedure.

• SOP is a set of step-by-step instructions that outline how to perform a specific task or procedure.

• It ensures consistency, quality, and compliance in research activities.

• SOPs are used in various fields, including clinical research, to ensure standardized practices.

• Examples of SOPs in clinical research include guidelines for participant recruitment, data collection, and adverse event reporting.

Clinical trials are research studies that test new treatments or interventions on human subjects.

• Phase I trials: test safety and dosage in a small group of healthy volunteers

• Phase II trials: test effectiveness and side effects in a larger group of patients with the condition being treated

• Phase III trials: compare the new treatment to the current standard of care in a large group of patients

• Phase IV trials: monitor the long-term safety and effectiveness of the treatment after ...read more