Ccrp test questions - Study guides, Class notes & Summaries

CCRP SOCRA Certification Proficiency knowledge test Exam Questions and certified Answers 2024/2025 Define dead fetus - correct answer a fetus that exhibits neither heartbeat, respiratory activities, muscle movements or pulsations of the umbilical cord Neonate - correct answer newborn Nonviable neonate - correct answer a neonate after delivery that although living is not viable Viable neonate - correct answer being able to survive after delivery (given the benefit of available medical...

CCRP Practice Questions with Approved Answers | Latest 2023/2024 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 Duri...

SOCRA CCRP 2023 Exam Questions and Answers All Correct FDA Part 11 - Answer-electronic signatures are of the same validity as handwritten signatures, must provide 2 identifiers and verify identification of signer FDA Part 50 - Answer-Food and Drugs, and ICF FDA Part 56 - Answer-IRBs FDA Part 312 - Answer-investigational new drug application FDA Part 812 - Answer-investigational drug exemption FDA Form 482 - Answer-Notice of inspection FDA Form 483 - Answer-Letter of investiga...

Significant risk device is defined as an investigational device that is: a. Intended as an implant and presents a potential for serious risk to the health, safety, or welfare of a subject. b. Purported or represented to be for a use in supporting or sustaining human life and presents a potential risk to the health, safety, or welfare of a subject. c. For a use of substantial importance in diagnosing, curing, mitigating, or treating disease, or otherwise preventing impairment of human health...

SOCRA CCRP Exam Practice Questions and answers, VERIFIED/ 21 CFR part 11 regulates? - -Electronic Signatures What is the name of FDA Form 483? - -Inspectional Observation What does 21CFR56 regulate? - -Institutional Review Boards An application for Investigational Device Exemption is part of 21 CFR part ____________? - -812 Define Electronic Signature - -A computer data compilation of any symbol or series of symbols executed, adopted, or authorized by an individual to be legally binding...

CCRP AACVPR EXAM| 842 Exam TEST BANK with Questions and 100% Correct Answers| Graded A+

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SOCRA CCRP Final Competency Certification Study Guide Exam Questions with Certified for Accuracy Answers 2024/2025 Per ICH E8, methods used to evaluate patient usage of the test drug should be what? - correct answer Specified in the protocol and actual usage documented The study subject asks you why the study is called a double-blind study. You explain double blind as what? - correct answer When the subject and the Investigator and sponsor staff who are involved in the treatment or clinica...