<--- Back to Details
First PageDocument Content
Law / Foreign relations / Government / Intellectual property law / Pharmaceutical industry / Marketing authorization / Pharmaceuticals policy / European Patent Organisation / Supplementary protection certificate / Patent / European Patent Convention / Trademark
Law
Foreign relations
Government
Intellectual property law
Pharmaceutical industry
Marketing authorization
Pharmaceuticals policy
European Patent Organisation
Supplementary protection certificate
Patent
European Patent Convention
Trademark

Application for grant of a Supplementary Protection Certificate for Plant Protection Products Please consult the Guide for filling in the Application for grant of a Supplementary Protection Certificate for Plant Protecti

Add to Reading List

Source URL: iprights.dkpto.org

Download Document from Source Website

File Size: 400,42 KB

Share Document on Facebook

Similar Documents

Medical research / Clinical research / Health / Multi-speed Europe / Clinical data management / EudraCT / Clinical pharmacology / European Economic Area / Clinical Trials Directive / Clinical trial / Supplementary protection certificate

Trial results: Modalities and timing of posting VersionAprilInterventional Clinical Trials that ended on or after 21 Julyi.e. the date of finalisation of the programming according to Commission Gui

DocID: 1r4sk - View Document

emea_strap_url_cmyk_rev_en_std_cent.eps MASTER

emea_strap_url_cmyk_rev_en_std_cent.eps MASTER

DocID: 1qVx6 - View Document

Question Q202 National Group: Sweden Suède Schweden  Title:

Question Q202 National Group: Sweden Suède Schweden Title:

DocID: 1qeRN - View Document

B.12 AF user guide consolidated vet version EMA

B.12 AF user guide consolidated vet version EMA

DocID: 1pz2w - View Document

Clinical research / Pharmaceutical industry / Clinical data management / Drug safety / Electronic common technical document / Supplementary protection certificate / European Medicines Agency / Summary of Product Characteristics / Pharmacovigilance / Validation / Drug Master File

DOC Document

DocID: 1oZjJ - View Document