I opened a new submission for a Scientific Advice for an MRP product and I have a question concerning the procedural information.
When it asks for the marketing authorisation status, should I choose 'Yes' or 'No'?
I believe the answer would be No, as it only applies for centrlised procedures. But then, there is a field asking for the MRP procedures numbers. I am attaching an screenshot of the fields.
However, if I say yes, in the firts field, only the centralised products appear and there is not an option of 'Not applicable'.
Could you clarify that?
