Rac us devices - Study guides, Class notes & Summaries

US RAC Review Questions RAPS Modules With Complete Solutions Latest 2023/2024 (100% Verified). drug, which of the following studies would typically be conducted first: A) 1 month repeat dose toxicology study B) Single dose escalation PK study in healthy volunteers C) Multiple dose PK study in healthy volunteers D) Single dose escalation study in hypertensive patients:  B) Single dose esca- lation PK study in healthy volunteers 3. A sponsor must report an unexpected, fatal or life...

US RAC Review Questions RAPS Modules With Complete Solutions (Latest Update) 2023 | Verified Answers. 1. 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 u...

US RAC Review Questions RAPS Modules With Complete Solutions Latest Update 2023/2024 (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 us...

DEVICE RAC EXAM - Questions and Answers (Complete Solutions) Which division would have primary jurisdiction over a vascular graft with an antibiotic based on primary mode of action? A. CDER B. CBER C. CDRH D. OCP A company wants to modify its legally marketed device such that the modification does not affect the intended use or alter the fundamental scientific technology of the device. If the design outputs of the modified device meet the design input requirements, this change would be best fil...

Regulations - interpret laws and describe how they will be enforced guidance document - used to convey FDA's current thinking or enforcement priorities - not legally binding Sherley Amendment - prohibited labeling medicines with false therapeutic claims intended to defraud the purchaser Pure Food and Drug Act of 1906 - prohibited misbranded and adulterated foods, drinks and drugs from entering interstate commerce FD&C Act - 1938 - repealed 1906 law and sherley amendment - manufacturers w...

RAC Device Exam Questions and answers Graded A+ What did the safe medical device act do? - ANSExtended AE reporting to user facilities, required 510ks with SE, recall authority General controls - ANSEstablishment reg and device listing, GMP, labels, clearance before marketing What controls are required by the 3 US classes? - ANSClass 1 - general controls. Class 2- General and special controls (which include special labeling, PMS, and performance data) Class 3- general, special, and PMA ...

US RAC Review Questions RAPS Modules With Complete Solutions (Latest Update) 2023 | Verified Answers. 1. 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 u...

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...

RAC Exam Prep 2023 International Regulatory Qs&As Members of IMDRF - ANS-Australia, Brazil, Canada, China, Europe, Japan, Russia, Singapore, S. Korea, US What types of evaluations are typical variable from nation to nation? - ANS-Performance and clinical evaluations What is the Helsinki Declaration? - ANS-statement of ethical principles for medical research involving humans What are the 5 elements of a conformity assessment? - ANS-1. QMS 2. PMS 3. Technical doc summary 4. Declarati...

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