RAC Bundled Exams Together with complete solutions Questions and Answers Graded A, Latest Update (Verified Answers) (Full Solution Pack)
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DEVICE RAC EXAM 2024 | 70 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ 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 - C A company wants to modify its leg...
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Add to cartDEVICE RAC EXAM 2024 | 70 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ 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 - C A company wants to modify its leg...
DEVICE RAC EXAM 2024 | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ 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 - C A company wants to modify its legall...
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Add to cartDEVICE RAC EXAM 2024 | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ 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 - C A company wants to modify its legall...
RAC device quiz 2024 | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ EU: Which of the following does NOT describe the CE Mark or its use? A)The CE Mark is an external indication that a device meets the Essential Requirements B)The manufacturer and/or the Notified ...
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Add to cartRAC device quiz 2024 | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ EU: Which of the following does NOT describe the CE Mark or its use? A)The CE Mark is an external indication that a device meets the Essential Requirements B)The manufacturer and/or the Notified ...
RAC devices EU 2024 | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ regulations - legally binding and directly enforceable directives - legally binding but just be transposed into national law each country can decide how they want to implement medical device dir...
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Add to cartRAC devices EU 2024 | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ regulations - legally binding and directly enforceable directives - legally binding but just be transposed into national law each country can decide how they want to implement medical device dir...
RAC DEVICES Exam Prep 2024 | 60 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ A company is performing routine site monitoring of its pivotal clinical study for a blood sugar meter and finds one site has not consented one-third of its subjects properly . What is the ...
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Add to cartRAC DEVICES Exam Prep 2024 | 60 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ A company is performing routine site monitoring of its pivotal clinical study for a blood sugar meter and finds one site has not consented one-third of its subjects properly . What is the ...
RAC Devices Exam Prep 2024 (EU) | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ Who is the European Medicines Agency (EMA) - an agency of the European Union (EU) in charge of the evaluation and supervision of medicinal products. The primary reason for establishing E...
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Add to cartRAC Devices Exam Prep 2024 (EU) | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ Who is the European Medicines Agency (EMA) - an agency of the European Union (EU) in charge of the evaluation and supervision of medicinal products. The primary reason for establishing E...
RAC Prep Medical Devices 2024 | 70 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ device - instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent or related article: -recognized by NF-USP -intended for use in diagnosis of disease or other...
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Add to cartRAC Prep Medical Devices 2024 | 70 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ device - instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent or related article: -recognized by NF-USP -intended for use in diagnosis of disease or other...
FDA Time Frames (Device) RAC Exam 2024 | 35 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ Facility Registration - Devices - within XX days of application or manufacturing - 30 days Facility Re-Registration - Devices, Drugs & Biologics - Annual GLP & GCP Record Ret...
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Add to cartFDA Time Frames (Device) RAC Exam 2024 | 35 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ Facility Registration - Devices - within XX days of application or manufacturing - 30 days Facility Re-Registration - Devices, Drugs & Biologics - Annual GLP & GCP Record Ret...
RAC sample exam 2024 | 130 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ Side A - Side B Which of the following was NOT a requirement of the original Food, Drug, and Cosmetic Act of 1938? a) Proof of efficacy b) Proof of safety c) Authorized standards of identif...
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Add to cartRAC sample exam 2024 | 130 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ Side A - Side B Which of the following was NOT a requirement of the original Food, Drug, and Cosmetic Act of 1938? a) Proof of efficacy b) Proof of safety c) Authorized standards of identif...
RAC Practice Exam 1 2024 | 93 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ 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 a...
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Add to cartRAC Practice Exam 1 2024 | 93 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ 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 a...
2024 RAC Practice Exam | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ A physician reports to a manufacturer that a patient was hospitalized with acute sepsis after treatment with an approved device. This side effect is not listed in the package insert. This event m...
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Add to cart2024 RAC Practice Exam | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ A physician reports to a manufacturer that a patient was hospitalized with acute sepsis after treatment with an approved device. This side effect is not listed in the package insert. This event m...
RAC 2016 US RAC Practice Exam 2024 | 100 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ A physician reports to a manufacturer that a patient was hospitalized with acute sepsis after treatment with an approved device. This side effect is not listed in the package inse...
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Add to cartRAC 2016 US RAC Practice Exam 2024 | 100 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ A physician reports to a manufacturer that a patient was hospitalized with acute sepsis after treatment with an approved device. This side effect is not listed in the package inse...
US RAC Exam Prep 2024 | 175 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ 30-day hold - (aka 30-day safety review) Time frame between filing a protocol under an IND and the FDA approval to proceed with enrollment. Also, the time period between when a company submits...
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Add to cartUS RAC Exam Prep 2024 | 175 Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ 30-day hold - (aka 30-day safety review) Time frame between filing a protocol under an IND and the FDA approval to proceed with enrollment. Also, the time period between when a company submits...
RAC Devices Exam Prep-US High Risk 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ Number of Days for review of PMA - 180 days How many routes to a PMA? - 3 Routes: 1. 2 3 What makes a PMA unique (vs 510k)? - -Must include section on clinical investigations on...
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Add to cartRAC Devices Exam Prep-US High Risk 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ Number of Days for review of PMA - 180 days How many routes to a PMA? - 3 Routes: 1. 2 3 What makes a PMA unique (vs 510k)? - -Must include section on clinical investigations on...
RAC Sample Test 2024 | 100 Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ Which of the following is considered part of the Device Master Record? A. Employee training record B. Labeling specifications C. Design reviews D. Calibration records - B. Labeling specificatio...
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Add to cartRAC Sample Test 2024 | 100 Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ Which of the following is considered part of the Device Master Record? A. Employee training record B. Labeling specifications C. Design reviews D. Calibration records - B. Labeling specificatio...
US RAC Review Questions RAPS Modules 2024 | 90 Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ 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 approve...
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Add to cartUS RAC Review Questions RAPS Modules 2024 | 90 Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ 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 approve...
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EU RAC Exam 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ protocol is approved to ensure what? - That it meets applicable quality and study design requirements. First course of action to market a new class III medical device technology in the shortest time is......
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Add to cartEU RAC Exam 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ protocol is approved to ensure what? - That it meets applicable quality and study design requirements. First course of action to market a new class III medical device technology in the shortest time is......
RAC Exam practice 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ Which of the following was NOT a requirement of the original Food Drug and Cosmetic Act of 1938? a) Proof of efficacy b) Proof of safety c) Authorized standards of identify d) Safe tolerances for una...
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Add to cartRAC Exam practice 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ Which of the following was NOT a requirement of the original Food Drug and Cosmetic Act of 1938? a) Proof of efficacy b) Proof of safety c) Authorized standards of identify d) Safe tolerances for una...
RAC Drugs Exam 2024 | 195 Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ Acceptance Criteria - A set of conditions that are met before deliverables are accepted. Accept - The act of formally receiving or acknowledging something and regarding it as being true, sound, sui...
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Add to cartRAC Drugs Exam 2024 | 195 Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ Acceptance Criteria - A set of conditions that are met before deliverables are accepted. Accept - The act of formally receiving or acknowledging something and regarding it as being true, sound, sui...
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RAC Drugs Final Exam 2024 | 40 Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ (EU) MA - Market Authorization or product license issued by health authority. Valid for 5 years and subject to 1 renewal. 4 EU procedures to obtain an MA - National, centralised, mutual recogn...
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Add to cartRAC Drugs Final Exam 2024 | 40 Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ (EU) MA - Market Authorization or product license issued by health authority. Valid for 5 years and subject to 1 renewal. 4 EU procedures to obtain an MA - National, centralised, mutual recogn...
RAC Drugs Final Exam Study Guide 2024 | 45 Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ (EU) MA - Market Authorization or product license issued by health authority. Valid for 5 years and subject to 1 renewal. 4 EU procedures to obtain an MA - National, centralised, m...
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Add to cartRAC Drugs Final Exam Study Guide 2024 | 45 Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ (EU) MA - Market Authorization or product license issued by health authority. Valid for 5 years and subject to 1 renewal. 4 EU procedures to obtain an MA - National, centralised, m...
RAC Exam Questions - NJ Edits. 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ Procedure for submission of an application requiring investigations for approval of a new indication for, or other change from, a listed drug. 505 (B) 1 &2 - 21 CFR 314.54 WHAT CAN'T B...
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Add to cartRAC Exam Questions - NJ Edits. 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ Procedure for submission of an application requiring investigations for approval of a new indication for, or other change from, a listed drug. 505 (B) 1 &2 - 21 CFR 314.54 WHAT CAN'T B...
RAC ROOTS 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ nasc/nat - birth/born mentor words: nation, international ten/tain - hold mentor words: contain, retain fer - carry/bear mentor words: ferry, transfer pos/pon - put/place mentor words: position, depos...
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Add to cartRAC ROOTS 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ nasc/nat - birth/born mentor words: nation, international ten/tain - hold mentor words: contain, retain fer - carry/bear mentor words: ferry, transfer pos/pon - put/place mentor words: position, depos...
RAC Exam 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ drug - Any article intended for use in the diagnosis, cure, mitigation, treatment or prevention of disease in man. medical device - An instrument, apparatus, implement, machine, contrivance, implant, in vitr...
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Add to cartRAC Exam 2024 | Questions with 100% Correct Answers | Verified | Latest Update | Graded A+ drug - Any article intended for use in the diagnosis, cure, mitigation, treatment or prevention of disease in man. medical device - An instrument, apparatus, implement, machine, contrivance, implant, in vitr...
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