<--- Back to Details
First PageDocument Content
Pharmaceutical industry / Patent law / Law / Intellectual property law / Test data exclusivity / Supplementary protection certificate / Biosimilar / Generic drug / European Medicines Agency / Pharmaceutical sciences / Pharmacology / Pharmaceuticals policy
Date: 2010-10-13 11:07:56
Pharmaceutical industry
Patent law
Law
Intellectual property law
Test data exclusivity
Supplementary protection certificate
Biosimilar
Generic drug
European Medicines Agency
Pharmaceutical sciences
Pharmacology
Pharmaceuticals policy

Add to Reading List

Source URL: ec.europa.eu

Download Document from Source Website

File Size: 2,60 MB

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

Pharmaceuticals policy / Health / Pharmaceutical industry / Pharmacology / European Medicines Agency / European Union / Marketing authorization / European Directorate for the Quality of Medicines / EudraLex / European Pharmacopoeia / Orphan drug / Supplementary protection certificate

emea_strap_url_cmyk_rev_en_std_cent.eps MASTER

DocID: 1qVx6 - View Document

Law / Government / Foreign relations / Patent law / United States patent law / Compulsory license / Patent application / Patent / European Patent Convention / Unitary patent / Supplementary protection certificate / Term of patent in the United States

Question Q202 National Group: Sweden Suède Schweden Title:

DocID: 1qeRN - View Document

Pharmaceuticals policy / Pharmaceutical industry / Council of Europe / European Directorate for the Quality of Medicines / Marketing authorization / Bioequivalence / Test data exclusivity / European Medicines Agency / Supplementary protection certificate

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