Attero Recycling Interview Questions and Answers

Informed consent form and process is a legal and ethical requirement in clinical research that ensures participants are fully informed about the study and voluntarily agree to participate.

• Informed consent is a process where the researcher provides detailed information about the study to the participant.

• The participant must have the capacity to understand the information provided and make an informed decision.

• The informed consent form is a written document that outlines the pu...read more

A coronary stent is a small metal mesh tube used to treat narrowed or blocked arteries in the heart.

• It is inserted into the artery via a catheter

• It expands to keep the artery open and improve blood flow

• It is often used in patients with coronary artery disease or after a heart attack

• There are different types of stents, including bare metal stents and drug-eluting stents

• Complications can include blood clots or re-narrowing of the artery

Myocardial infarction is the medical term for a heart attack.

• It occurs when the blood flow to a part of the heart is blocked, usually by a blood clot.

• Symptoms include chest pain, shortness of breath, and sweating.

• Immediate medical attention is necessary to prevent further damage to the heart.

• Treatment may include medications, surgery, or lifestyle changes to prevent future heart attacks.

An investigator site file contains essential documents related to the clinical trial conducted at the site.

• Curriculum vitae of the investigator and other staff members

• Signed investigator agreement

• Ethics committee approval

• Informed consent forms

• Protocol and amendments

• Investigational product information

• Adverse event reports

• Monitoring reports

• Financial disclosure forms

• Site delegation log

Good clinical practice refers to ethical and scientific standards for designing, conducting, recording, and reporting clinical trials.

• GCP ensures the safety and well-being of trial participants

• It ensures the reliability and credibility of trial results

• It involves adherence to ethical principles and regulatory requirements

• It requires proper documentation and record-keeping

• Examples of GCP guidelines include ICH-GCP and FDA regulations

EC dossier is prepared by compiling all necessary documents related to clinical trial and submitting to Ethics Committee.

• Compile all necessary documents such as protocol, informed consent form, investigator brochure, etc.

• Ensure all documents are up-to-date and in compliance with regulatory guidelines.

• Include a cover letter explaining the purpose of the submission and any relevant information.

• Submit the dossier to the appropriate Ethics Committee for review and approval.

• Addres...read more

The heart is a muscular organ that pumps blood throughout the body, providing oxygen and nutrients to the tissues.

• The heart is located in the chest, between the lungs and behind the sternum.

• It has four chambers: the right atrium, right ventricle, left atrium, and left ventricle.

• The right side of the heart receives deoxygenated blood from the body and pumps it to the lungs for oxygenation, while the left side receives oxygenated blood from the lungs and pumps it to the rest of...read more