What is gcp - Study guides, Class notes & Summaries
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SOCRA EXAM PREP | 2023/ 2024 Newly Updated | ALL EXAMS COMBINED| Questions and Verified Answers| Highly Rated Guide
- Exam (elaborations) • 356 pages • 2023
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SOCRA EXAM PREP | 2023 Update | Questions and Verified Answers| Highly Rated Guide 
 
Q: What 4 aspects of a trial should a sponsor focus on when monitoring for compliance per 21 CFR 312.56? 
 
Answer: 
1) Progress of investigations under IND 
2) Secure compliance or discontinue investigators that are not compliant and notify FDA 
3) Review safety/effectiveness of drug and report safety issues to FDA + make annual reports or progress 
4) Notify FDA, all IRBs and all investigators if drug presen...
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Pharmaschool.co ICH GCP 106 Questions And Answers Graded A+
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According to ICH GCP what are the absolute minimum requirements for essential documents at site 
before IMP can be sent to the site? 
a. CV of investigator and Clinical Trial Authorization (CTA) 
b. Ethics Committee Approval and signed protocol 
c. CTA and Ethics Committee Approval 
d. CTA, Ethics Committee Approval and signed protocol - c. CTA and Ethics Committee Approval 
What C is missing from this statment in ICH GCP: The sponsor should provide insurance or should 
indemnify (legal and fina...
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ACRP Boot camp Exam Questions and Answers Already Passed
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ACRP Boot camp Exam Questions and Answers Already Passed 
The clinical trial phase that focuses on safety and human pharmacology in healthy volunteers is: 
a. phase 1 
b. phase 2 
c. phase 3 d. phase 4 a 
Which of the following is not a type of patient-oriented research? 
a. IND/IDE clinical trials 
b. investigator initiated trial (IIT) 
c. Post market device registries d. outcome and health services research d 
Who is ultimately responsible for all aspects of the research conducted at a site? 
...
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Pharma school ICH GCP Questions with correct answers
- Exam (elaborations) • 18 pages • 2023
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According to ICH GCP what are the absolute minimum requirements for essential documents at site before IMP can be sent to the site? 
 
a. CV of investigator and Clinical Trial Authorization (CTA) 
b. Ethics Committee Approval and signed protocol 
c. CTA and Ethics Committee Approval 
d. CTA, Ethics Committee Approval and signed protocol CORRECT ANSWER c. CTA and Ethics Committee Approval 
 
What C is missing from this statement in ICH GCP: The sponsor should provide insurance or should indemnify...
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Good Clinical Practice ICH exam 2023 with 100% correct answers
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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...
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ACRP CCRC Exam Prep Questions and answers 100% correct
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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...
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SOCRA- 2022 QUESTIONS AND ANSWERS ALL CORRECT
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Belmont Report was created as part of? Correct Answer: The national Research Act of 1974. 
 
Who was the Belmont Report formulated by? Correct Answer: The National Commission for the protection of human subjects in biomedical and behavioral research. 
 
What year was the publication of the FDA regulations made? Correct Answer: 1980 *1981 for the HHS and revised FDA Regulations. 
 
What year was GCP and HIPAA created? Correct Answer: 1996 
 
What is the National Research Act? Correct Answer: ...
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GCP EXAM QUESTIONS AND ANSWERS 100% CORRECT
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GCP EXAM QUESTIONS AND ANSWERS 100% CORRECT 
What words are missing from the following in ICH GCP: The Sponsor should update the XXXX as significant new information becomes available? 
investigator's brochure 
 
 
 
Who is responsible for implementing and maintaining quality assurance and quality control systems with written SOPs: 
sponsor 
 
 
 
According to ICH GCP section 8, what is the purpose of IRB/IEC composition? 
A. To document that the IRB/IEC is constituted in agreement with GCP 
 
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SoCRA Certification Exam 2023 with complete answers
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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...
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Mastering Terraform: A practical guide to building and deploying infrastructure on AWS, Azure, and GCP
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Mastering Terraform: A practical guide to building and deploying infrastructure on AWS, Azure, and GCP 
 
What you will learn 
Explore Terraform architecture and configurations in depth 
Integrate Packer with Terraform for VM-based solutions 
Containerize apps with Docker and Kubernetes 
Explore GitOps and CI/CD deployment patterns 
Transform existing applications into serverless architectures 
Migrate and modernize legacy apps for the cloud 
Implement Terraform on AWS, Azure, and GCP 
Use Terra...
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