Aequs Engineered Plastics Interview Questions and Answers

LAR stands for Last Available Record while IW stands for Interim Withdrawal.

• LAR refers to the last data point collected before a participant drops out of a study.

• IW refers to a participant withdrawing from a study before its completion.

• LAR is used in statistical analysis while IW is used in safety analysis.

• LAR is also known as LLOQ (Last Locus of Observation Quantifiable).

I am not currently involved in a clinical trial, so I cannot provide information on AE's and SAE's.

• Not involved in a clinical trial at present

• Cannot provide information on AE's and SAE's

ICF stands for Informed Consent Form, a document that explains the study to potential participants.

• ICF is a legal document that outlines the study's purpose, procedures, risks, and benefits.

• It also explains the participant's rights and responsibilities.

• ICF must be signed by the participant or their legally authorized representative before they can participate in the study.

• ICF is an essential part of the ethical conduct of clinical research.

• ICF must be written in a language th...read more

Clinical research involves conducting studies to evaluate the safety and effectiveness of new medical treatments, drugs, or devices.

• Clinical research aims to gather data on the benefits and risks of new medical interventions.

• It involves recruiting participants, collecting data, and analyzing results to determine the efficacy of the intervention.

• Clinical research is essential for advancing medical knowledge and improving patient care.

• Examples of clinical research include drug ...read more

ICH GCP stands for International Conference on Harmonisation Good Clinical Practice.

• ICH GCP is a set of international standards for the design, conduct, performance, monitoring, auditing, recording, analysis, and reporting of clinical trials.

• It ensures that the rights, safety, and well-being of trial subjects are protected and that the clinical trial data is credible.

• Adherence to ICH GCP guidelines is mandatory for conducting clinical trials in many countries.

• Examples of ICH ...read more

Clinical trials typically have four phases: Phase 1, Phase 2, Phase 3, and Phase 4.

• Phase 1: Small group of healthy volunteers to test safety and dosage

• Phase 2: Larger group to further evaluate safety and effectiveness

• Phase 3: Even larger group to confirm effectiveness, monitor side effects, and compare to existing treatments

• Phase 4: Post-marketing studies to monitor long-term effects and benefits