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Documents Bundesinstitut für Arzneimittel und Medizinprodukte Pt WHO-consultant 1 World Health Organization.....

Slide 1Bundesinstitut für Arzneimittel und Medizinprodukte Pt WHO-consultant 1 World Health Organization Training Workshop on Pharmaceutical Quality, Good Manufacturing…

Documents Kiev, 04/12/2007 Analysis of EU MRP/DCP procedures regarding to generic applications Dr.Raimonds...

Slide 1Kiev, 04/12/2007 Analysis of EU MRP/DCP procedures regarding to generic applications Dr.Raimonds Lozda, FMS Baltic Ltd Slide 2 Kiev, 04/12/2007 EU Authorities National…

Business C5 second medical_use_patents_presentation_29_january_2014

1. Second and further medical use patents: enforcement perspectiveDr Duncan Curley Director and Head of Patents, Innovate Legal C5 Pharma & Biotech Patent Litigation…

Health & Medicine Regulatory Perspectives on Biosimilars in Europe

Bruno Flamion, MD, PhD University of Namur Namur, Belgium NDA Advisory Group Past Chair of the European Medicines Agency (EMA) Scientific Advice Group Regulatory perspectives…

Documents Fordham IP Conference 9 April, 2015 - Cambridge Biosimilar Patent Litigation – UK Perspective Dr.....

Slide 1 Fordham IP Conference 9 April, 2015 - Cambridge Biosimilar Patent Litigation – UK Perspective Dr Penny Gilbert Powell Gilbert LLP 1 Slide 2 A changing landscape.…

Documents Data protection and extension of patent rights TRIPS requirements & TRIPS-plus provisions Carlos...

Slide 1 Data protection and extension of patent rights TRIPS requirements & TRIPS-plus provisions Carlos Correa Slide 2  Test data protection Slide 3 Medicines are…

Documents Implementation of Bioequivalence Study for Generic Medicines in Malaysia 2011

Implementation of Bioequivalence Study for Generic Medicines in Malaysia Centre For Product Registration National Pharmaceutical Control Bureau (NPCB) Ministry of Health…