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RAC DRUGS FINAL EXAM 2025| BRAND NEW ACTUAL EXAM WITH 100% VERIFIED QUESTIONS AND CORRECT SOLUTIONS| GUARANTEED VALUE PACK| ACE YOUR GRADES.

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RAC DRUGS FINAL EXAM 2025| BRAND NEW ACTUAL EXAM WITH 100% VERIFIED QUESTIONS AND CORRECT SOLUTIONS| GUARANTEED VALUE PACK| ACE YOUR GRADES.

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RAC DRUGS
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RAC DRUGS









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Institution
RAC DRUGS
Course
RAC DRUGS

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Uploaded on
March 7, 2025
Number of pages
6
Written in
2024/2025
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RAC DRUGS FINAL EXAM 2025| BRAND NEW ACTUAL
EXAM WITH 100% VERIFIED QUESTIONS AND
CORRECT SOLUTIONS| GUARANTEED VALUE PACK|
ACE YOUR GRADES.


1. (EU) MA - correct answer - Market Authorization or product license
issued by health authority. Valid for 5 years and subject to 1 renewal.




2. 4 EU procedures to obtain an MA - correct answer - National,
centralised, mutual recognition, decentralized procedures




3. MAH - correct answer - A legal person or legal entity who must be
established in the European Economic Area comprising of 28 member
states.




4. What does an MA include? - correct answer - Active substance
international non-proprietary name, trade name.




5. SmPC - correct answer - Summary of Product Characteristics




6. PIL - correct answer - Product Information Leaflet

, Page |2



7. 6 months - correct answer - How many months prior to expiration should
MA renewal be submitted?




8. Qualified Person (QP) in charge of? - correct answer -
Pharmacovigilance, scientific service in charge of each medicinal
products scientific info




9. ASMF - correct answer - Active Substance Master File, info regarding
the drug substance consists of one Applicants Part (AP), and one
Restricted Part (RP), or proprietary information.




10. CEP - correct answer - Certificate of Suitability




11. EDQM - correct answer - European Directory for the Quality of
Medicines




12. CTD Module 1 - correct answer - Region specific administrative data




13. CTD Module 2 - correct answer - Quality Overall Summary

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