Quality assurance gcp - Study guides, Class notes & Summaries

ICH GCP for CCRC Exam Prep|543 Questions and Answers 2023 Graded A+. Adverse Drug Reaction (ADR) Correct Answer: All noxious and unintended responses to a medicinal product related to any dose E6(R1) 1 Correct Answer: Glossary of terms Adverse Event (AE) Correct Answer: Any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and which does not necessarily have a causal relationship with this treatment--any unfavorable and uninten...

ACRP CCRC Exam Prep Questions and answers 100% correctWhat are expected or possible consequences of over-estimation of recruitment potential? - The trial will overrun its projected timeline - The recruitment period will be prolonged and more sites may be needed - The study will not have sufficient data within the required timeframe and will be stopped because of lack of budget What should be the first consideration when conducting a clinical trial? Subject welfare When is the i...

What is Good Clinical Practice (GCP)? An international ethical and scientific quality standard for designing, conducting, recording, and reporting trials that involve the participation of human subjects What does Good Clinical Practice assure? Assurance that the rights, safety, and well-being of trial subjects are protected, consistent with the principles that have their origin in the Declaration of Helsinki, and that the clinical trial data are credible. What is the objective G...

1A protocol that has been previously reviewed by the full IRB is always eligible for expedited review. A. TRUE B. FALSE - Answer-B. FALSE 1A serious adverse event (SAE) should be reported to the local IRB within what period of time after learning of the event? A. 5 days B. 2 weeks C. 24 hours D. Follow the local IRB reporting guidelines. - Answer-D. Follow the local IRB reporting guidelines. 1Essential documents collected for research projects may be audited or inspected for GCP complia...

SoCRA Certification Exam 2023 with complete answers Biometrics A method of verifying an individual's identity based on measurement of the individual's physical features or repeatable actions where those features and or actions are both unique to that individual and measurable. (21 CFR, Sec. 11.3) Closed System An environment in which system access is controlled by persons who are responsible for the content of electronic records that are on the system. (21 CFR, Sec. 11.3) Digi...

A company is performing routine site monitoring of its pivotal clinical study for a blood sugar meter and finds one site has not consented 1/3 of its subjects properly. What is the FIRST thing the company needs to do? A. Stop the entire study B. Inform FDA and ask for guidance C. Re-train the study staff, including the principle investigator at that site on GCP D. Re-consent all improperly consented subjects - D. Re-consent all improperly consented subjects The quality assurance manager o...

ACRP CCRC Study Guide (Latest 2024/ 2025 Update) Questions and Verified Answers| 100% Correct| Grade A Q: "Approval" (in relation to Institutional Review Boards) Answer: The affirmative de- cision of the IRB that the clinical trial has been reviewed and may be conducted at the institution site within the constraints set forth by the IRB, the institution, Good Clinical Practice (GCP), and the applicable regulatory requirements. Q: Audit Answer: A systematic and independent exa...

Socra Exam Prep With 100% Correct And Verified Answers Laws - Correct Answer-passed by national legislative bodies; establish authority of national regulatory body Regulations - Correct Answer-Passed by regulatory authorities; controls how medical products are investigated and approved; have effect of law guidance - Correct Answer-"current thinking" of regulatory bodies; non-binding ICH - Correct Answer-Developed to keep people doing things the same way across the world; internat...

declaration of helsinki (1964) correct answers-ethical principles (31) for research with human subjects -international standard -subjects take precedence -combing research and clinical care -adapted from Nuremberg Code by the World Medical Association ICH - international conference on harmonisation correct answersinternational authority on clinical research theory and principles ICH guidelines correct answers4 major categories QUALITY - chemical/pharm. Assurance (stability testin...