Remojudytask

18 years of age - ANSWER-Minimum age to become a Notary in PA 45 Days - ANSWER-What is maximum amount of time to record bond, oath of office and commission at the Recorder of Deeds in the county which the notary maintains an office? $10,000 - ANSWER-Under RULONA, what amount must surety bond from insurance company licensed in PA in? 30 Days - ANSWER-RULONA requires a surety company provide the Department of State how many days notice before canceling the bond? $1,000.00 - ANSWER-The ...

Minimum Age for becoming a Notary in PA - ANSWER-18 years of age ( Sec 321 a 1) Maximum time requirement for the bond, oath of office and commission to be recorded in the office of recorder of deeds of the county in which the Notary maintains an office - ANSWER-45 Days Under RULONA and applicant for a commission to obtain a surety bond from an insurance company licensed in PA in the order of the amount - ANSWER-$10,000 RULONDA requires a surety company or issuing entity of the bond to g...

SOCRA CCRP Exam Bundle Questions And Answers 100% Verified

Laws - ANSWER-passed by national legislative bodies; establish authority of national regulatory body Regulations - ANSWER-Passed by regulatory authorities; controls how medical products are investigated and approved; have effect of law guidance - ANSWER-"current thinking" of regulatory bodies; non-binding ICH - ANSWER-Developed to keep people doing things the same way across the world; international effort to harmonize the technical requirements for product registration SOPs - ANSW...

Which of the following is a disclosure of financial interests form? - ANSWER-FDA Form 3455 Which of the following is a certification of financial interest form? - ANSWER-FDA Form 3454 If the investigator did have financial arrangement with the sponsor, he/she would submit the following form: - ANSWER-FDA Form 3455 This form is submitted by sponsor to the FDA prior to the beginning of the drug trial - ANSWER-Investigational New Drug Application (1571) In the top right corner, form hav...

When was the Nuremberg Code created? - ANSWER-1947 What did the Nuremberg Code establish? - ANSWER-Worldwide requirement for informed consent with properly formulated experimentation with beneficence towards participants. When was Belmont report established? - ANSWER-1979 What does the Belmont report do? - ANSWER-- Establish boundaries between practice and research - created ethical principles: Respect for persons, Beneficence, and Justice - ensure applications of informed consent, ri...

A subject has been enrolled on a study and was randomized to the non-treatment arm. The protocol outlines study procedures for all subjects to be performed within one week of enrollment. Which of the following statements about this case is correct? a. This subject does not need to undergo any of the study procedures since the subject is enrolled on the non-treatment arm b. This subject should undergo all study procedures as outlined in the protocol c. This subject only needs to undergo the st...

What is an orphan drug program? - ANSWER-FDA program that provides development of drugs for rare diseases Nuremburg Code - ANSWER-set of standards proclaimed following the trial of Nazi doctors in 1947 Kefauver-Harris Amendment - ANSWER-Amendment to Food Drug and Cosmetic Act that requires informed consent for experimental drugs Adverse Event - ANSWER-any unfavorable or unintended event associated with a research study Assent - ANSWER-a child's affirmative agreement to participate i...

ACT - ANSWER-Federal food drug and cosmetic acts agency - ANSWER-Food and Drug Administration Biometrics - ANSWER-Method of verifying ID based on measurement of physical features, repeatable features, where those features and/or actions are both unique to that individual and measurable closed system - ANSWER-Environment in which the system access is controlled by persons who are responsible for the content of electronic records that are on the system open system - ANSWER-Environment ...

A sponsor who determines and unanticipated AE presents unreasonable risk, termination shall occur within _____ working days and not later than ___ working days after sponsor first received notice of effect - ANSWER-5, 15 IRB determinations for emergency situations are to be retained by IRB for at least ___ years after completion of clinical investigation - ANSWER-3 Al IRB records need to be kept for ____ years follow completion of research - ANSWER-3 FDA will provide written determinati...