Origin of petitions, by Member State (left) and Member States concerned
Concerned Member State. Web the member state that has already authorised the product is known as the reference member state (rms). A european economic area country in which an application has been submitted for.
Web the member state that has already authorised the product is known as the reference member state (rms). Web concerned member state a european economic area country in which an application has been submitted for. A european economic area country in which an application has been submitted for. The regulatory authority in whose territory a clinical trial with the imp is being conducted or is. Then, the applicant seeks approval for the.
The regulatory authority in whose territory a clinical trial with the imp is being conducted or is. Then, the applicant seeks approval for the. Web the member state that has already authorised the product is known as the reference member state (rms). A european economic area country in which an application has been submitted for. The regulatory authority in whose territory a clinical trial with the imp is being conducted or is. Web concerned member state a european economic area country in which an application has been submitted for.
