Ccrp practice question - Study guides, Class notes & Summaries

CCRP Practice Questions Prior to archiving a study, documentation of IP destruction at the site should be filed in the study files of the: - ANSWER-PI and Sponsor. In the case of an incapacitated subject, who should receive a copy of the signed and dated ICF? - ANSWER-The subject's legally acceptable representative Which of the following required elements should be included in a clinical trial protocol? - ANSWER-The subject inclusion and exclusion criteria During a multi-site clin...

CCRP Practice Questions with complete Answers 2023 Prior to archiving a study, documentation of IP destruction at the site should be filed in the study files of the: PI and Sponsor. In the case of an incapacitated subject, who should receive a copy of the signed and dated ICF? The subject's legally acceptable representative Which of the following required elements should be included in a clinical trial protocol? The subject inclusion and exclusion criteria During a mult...

CCRP Practice Questions Answered Correctly Prior to archiving a study, documentation of IP destruction at the site should be filed in the study files of the: - ANSWER PI and Sponsor. In the case of an incapacitated subject, who should receive a copy of the signed and dated ICF? - ANSWER The subject's legally acceptable representative Which of the following required elements should be included in a clinical trial protocol? - ANSWER The subject inclusion and exclusion criteria During ...

Prior to archiving a study, documentation of IP destruction at the site should be filed in the study files of the: - answerPI and Sponsor. In the case of an incapacitated subject, who should receive a copy of the signed and dated ICF? - answerThe subject's legally acceptable representative Which of the following required elements should be included in a clinical trial protocol? - answerThe subject inclusion and exclusion criteria During a multi-site clinical study, whose responsibility is...

CCRP Practice Questions and answers correctly 2023 Prior to archiving a study, documentation of IP destruction at the site should be filed in the study files of the: - answerPI and Sponsor. In the case of an incapacitated subject, who should receive a copy of the signed and dated ICF? - answerThe subject's legally acceptable representative Which of the following required elements should be included in a clinical trial protocol? - answerThe subject inclusion and exclusion criteria During...

CCRP Practice Questions and Answers (Latest 2023/2024) Verified Answers

Prior to archiving a study, documentation of IP destruction at the site should be filed in the study files of the: PI and Sponsor. In the case of an incapacitated subject, who should receive a copy of the signed and dated ICF? The subject's legally acceptable representative Which of the following required elements should be included in a clinical trial protocol? The subject inclusion and exclusion criteria During a multi-site clinical study, whose responsibility is it to...

CCRP Practice Questions | 100% Correct Answers | Verified | Latest 2024 Version Prior to archiving a study, documentation of IP destruction at the site should be filed in the study files of the: - PI and Sponsor. In the case of an incapacitated subject, who should receive a copy of the signed and dated ICF? - The subject's legally acceptable representative Which of the following required elements should be included in a clinical trial protocol? - The subject inclusion and exclusion crite...

CCRP IRB, ICH and FDA Practice Guide Exam Question and answers 2023/2024 How many days does a sponsor have to report an emergency use of an IP to the FDA? - correct answer 5 working days How many members must sit on an IRB? - correct answer 5 How long must an IRB retain records per 21 CFR 56? - correct answer 3 years after completion of research What are the criteria for IRB approval of research? (7) - correct answer 1. Risks to subjects are minimized 2. Risks are reasonable in relati...