Annexes to COM(2018)317 - Amendment of Regulation (EC) No 469/2009 concerning the supplementary protection certificate for medicinal products

Please note

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ANNEX

The following Annexes are inserted:

‘ANNEX -I

Logo

This logo shall appear in black and in such a size as to be sufficiently visible.


ANNEX -Ia

Standard form for notification pursuant to points (b) and (c) of Article 5(2)

Tick the appropriate box
New notification

Update of an existing notification
(a)Name and address of the maker
(b)Purpose of making
Export

Storing

Export and storing
(c)Member State in which making is to take place and Member State in which first related act (if any) prior to making is to take place
Member State of making
(Member State of first related act (if any))
(d)Number of certificate granted in the Member State of making and number of certificate granted in Member State of first related act (if any) prior to making
Certificate of Member State of making
(Certificate of Member State of first related act (if any))
(e)For medicinal products to be exported to third countries, reference number of marketing authorisation, or the equivalent of such authorisation, in each third country of export