Fda form 482 - Study guides, Class notes & Summaries

45 CFR 46 Subpart A - Correct Answer-"Basic HHS Policy for Protection of Human Research Subjects": (46.100) Requirements for 1) assuring compliance by research institutions, 2) researchers' obtaining and documenting informed consent, 3) Institutional Review Board (IRB) membership, function, operations, review of research, and record keeping. 45 CFR 46 Subpart B - Correct Answer-Additional protections for pregnant women, human fetuses, and neonates (46.200) 45 CFR 46 Subpart C - Correct...

Certified Clinical Research Professional (CCRP) Exam Questions Answered 100% correct When isn't an IND application needed? IND Application is not needed if investigation does not support change in labeling What information must the general IND include? (21 CFR Part 312.23) FDA Form 1571: -FDA Form 1571 cover sheet -Table of contents -Investigative plan -Investigator's brochure -Protocol -Chemistry/Manufacturing information -Pharmacology/toxicology -Previous human research/lit...

When isn't an IND application needed? - Answer IND Application is not needed if investigation does not support change in labeling What information must the general IND include? (21 CFR Part 312.23) - Answer FDA Form 1571: -FDA Form 1571 cover sheet -Table of contents -Investigative plan -Investigator's brochure -Protocol -Chemistry/Manufacturing information -Pharmacology/toxicology -Previous human research/literature information -Additional information (drug dependence and abuse ...

FDA Part 11 - electronic signatures are of the same validity as handwritten signatures, must provide 2 identifiers and verify identification of signer FDA Part 50 - Food and Drugs, and ICF FDA Part 56 - IRBs FDA Part 312 - investigational new drug application FDA Part 812 - investigational drug exemption FDA Form 482 - Notice of inspection FDA Form 483 - Letter of investigational observations/citation of noncompliance that specifies how long you have to respond. FDA Form 3454 - Certific...

SOCRA Practice 1 questions and answers latest 2023 True or False The terms "treatment protocol" and "treatment IND" are interchangeable and mean the same thing. False. A treatment protocol is sponsored by a sponsor, while a treatment IND (Investigational New Drug) is sponsored by a licensed medical practitioner who becomes a sponsored investigator. 21 CRF 312.35 True or False Investigators are responsible for periodically requesting updates regarding new information gleaned by a ...

SOCRA Practice Test questions and answers with complete top solutions Which of the following is a disclosure of financial interests form? FDA Form 3455 Which of the following is a certification of financial interest form? FDA Form 3454 If the investigator did have financial arrangement with the sponsor, he/she would submit the following form: FDA Form 3455 This form is submitted by sponsor to the FDA prior to the beginning of the drug trial Investigational New Drug Appl...

SOCRA Certification Exam with complete top solutions,A+ test Does the FDA consider electronic signatures to be as trustworthy and reliable as handwritten paper signatures? Yes (although permission to use such e-sigs has to be approved by the FDA) Does the FDA consider electronic records that meet requirements to be equivalent to handwritten records ? Yes Open system (FDA term) System access is NOT controlled by people who are responsible for the content of the electronic recor...

SOCRA- 2023 100% accurate answers Belmont Report was created as part of? The national Research Act of 1974. Who was the Belmont Report formulated by? The National Commission for the protection of human subjects in biomedical and behavioral research. What year was the publication of the FDA regulations made? 1980 *1981 for the HHS and revised FDA Regulations. What year was GCP and HIPAA created? 1996 What is the National Research Act? A set of regulations for the...

When isn't an IND application needed? IND Application is not needed if investigation does not support change in labeling What information must the general IND include? (21 CFR Part 312.23) FDA Form 1571: -FDA Form 1571 cover sheet -Table of contents -Investigative plan -Investigator's brochure -Protocol -Chemistry/Manufacturing information -Pharmacology/toxicology -Previous human research/literature information -Additional information (drug dependence and abuse potential) ...

Certified Clinical Research Professional (CCRP) Exam correctly answered 2023When isn't an IND application needed? IND Application is not needed if investigation does not support change in labeling What information must the general IND include? (21 CFR Part 312.23) FDA Form 1571: -FDA Form 1571 cover sheet -Table of contents -Investigative plan -Investigator's brochure -Protocol -Chemistry/Manufacturing information -Pharmacology/toxicology -Previous human research/literature in...