21 cfr part 11 subpart b Study guides, Class notes & Summaries

US RAC Questions With Complete Solutions Latest Update 2024 (100% Verified Answers) In which situation is an IND not required? A) You intend to conduct a clinical trial with an investigational new drug B) You intend to conduct a clinical trial with an approved drug to support a marketing application for a new indication C) You intend to collect blood samples from subjects to look for biomarkers or pharmacogenetic information D) You intend to conduct a clinical trial using 2 of your approve...

CCRP SoCRA Exam 2024

SOCRA CCRP Exam Practice Test Questions With Complete Solutions 21 CFR part 11 regulates? - ANSWER Electronic Signatures What is the name of FDA Form 483? - ANSWER Inspectional Observation What does 21CFR56 regulate? - ANSWER Institutional Review Boards An application for Investigational Device Exemption is part of 21 CFR part ____________? - ANSWER 812 Define Electronic Signature - ANSWER A computer data compilation of any symbol or series of symbols executed, ...

Which of the following is NOT required for compliance under 21 CFR Part 11 (electronic records and electronic signatures)? A Manually generated timestamped audit trails to record the date and time of operator entries and actions that create, modify or delete electronic records. B Validation of systems to ensure accuracy C Authority checks to ensure that only authorized personell can create, modify or delete electronic records. D Establishment of and adherence to written procedures - ...

SOCRA CCRP Certification Exam Questions With Complete Solutions CFR Title 21: Part 11 - ANSWER Electronic Records; Electronic Signatures Part 11, Subpart A: General Provisions - ANSWER -must be trustworthy, reliable, and generally equivalent to paper records -applies to electronic forms that are created, modified, maintained, archived, retrieved, or transmitted -where records meet requirements, it will be considered equivalent to full handwritten signatures, initials, etc....

CON 090 FAR FUNDAMENTALS Exam Questions and Answers | Latest Update | 100% Verified. Where can I find the FAR? The FAR is available in print from the Government Printing Office as part of the Code of Federal Regulations, or from private publishers. However, it is arguably most conveniently accessed online, where it is available in either PDF or HTML format, at An unofficial version of the FAR is also available at . 3. What agencies are subject to the FAR? The FAR applies to most executiv...

CON 090 FAR FUNDAMENTALS EXAM Questions and Answers | Latest Update 2023- 2024 | Graded A+. CON 090 is a very rigorous course, and it will require a considerable amount of focused effort and discipline on your part to be successful. CON 090 will most likely be quite different than any other class you have taken before, and it is also very likely that nothing has prepared you for reading, interpreting, and applying the FAR and DFARS. Therefore to be successful, you must also develop the habit...

US RAC Review Questions and Answers RAPS Modules 2023 with complete solution In which situation is an IND not required? A) You intend to conduct a clinical trial with an investigational new drug B) You intend to conduct a clinical trial with an approved drug to support a marketing application for a new indication C) You intend to collect blood samples from subjects to look for biomarkers or pharmacogenetic information D) You intend to conduct a clinical trial using 2 of your approved dr...

Which of the following is NOT required for compliance under 21 CFR Part 11 (electronic records and electronic signatures)? A Manually generated timestamped audit trails to record the date and time of operator entries and actions that create, modify or delete electronic records. B Validation of systems to ensure accuracy C Authority checks to ensure that only authorized personell can create, modify or delete electronic records. D Establishment of and adherence to written procedures - correct ...

CCRP SOCRA Exam VERIFIED CFR Part 11 Electronic Records; Electronic Signatures 21 CFR Part 11 Subpart B Electronic Records 21 CFR Part 11 Subpart C Electronic Signatures 21 CFR Part 50 Protection of Human Subjects 21 CFR Part 50 Subpart B Informed Consent of Human Subjects 21 CFR Part 50 Subpart D Additional Safeguards for Children in Clinical Investigations 21 CFR Part 56 Institutional Review Board 21 CFR Part 56 Subpart B Organization and Personnel ...