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Course 5 Final Quiz
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Question 1 of 7
1. Question
The European Medicines Agency (EMA)
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Question 2 of 7
2. Question
A Marketing Authorisation for a new medicine
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Question 3 of 7
3. Question
When patients are involved in EMA activities they do so as an:
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Question 4 of 7
4. Question
Information contained within a package leaflet is intended for
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Question 5 of 7
5. Question
When a pharmaceutical company would like to obtain an authorisation for a cancer medicine they apply via:
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Question 6 of 7
6. Question
A new centrally authorised medicine must be made available in:
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Question 7 of 7
7. Question
Patients are involved at the EMA during which regulatory phases?
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