Ccrp practic - Study guides, Class notes & Summaries

SOCRA CCRP Practice Study Guide Questions with Distinction level Marking scheme version 2024/2025 What is a CAPA?? - correct answer Corrective and Preventative Action. It is a process to identify root cause of issues or problems and actions to resolve them.. CAPA plan is a document that describes the CAPA process. What is quality assurance? - correct answer Planned and systematic activities necessary to ensure that the trial is performed and the data are generated and in compliance with GC...

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

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 report subj...

CCRP Practice Questions and Answers All Correct 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 Dur...

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 c...

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...

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 report subj...

CCRP PRACTICE EXAM 2024/ QUESTIONS WITH CORRECT DETAILED /VERIFIED|