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EVENTS
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ABOUT US
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LEARNING SPACE
Learning Space
Companies face different situations today when moving into a strategic approach to IP management. This white paper aims to summarize these situations and reflects the views of ~400 IP and innovation professionals working in IP and innovation (R&D, R&I or the like) departments in a wide range of companies (large and SMEs), patent law firms and other organizations. The document is a compilation of both positive and less positive experiences, i.a. on the design, the implementation and the execution of the IP plan.
Download now the white paper 'IP strategy'.
Editor: Patentopolis B.V.
This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
Mit diesem Qualifikationslehrgang können Sie sich in allen Regulatory Affairs-Themen Medizinprodukte strukturiert weiterbilden und dabei fachliche Schwerpunkte legen. Eine detallierte Übersicht über den Lehrgang finden Sie in unserem <a href="https://www.forum-institut.de/public/Katalog Qualifikationslehrgang RA Manager.pdf" target="_blank"><b>Katalog</b> </a>.
Ihre Essentials bei In-vitro-Diagnostika: Unsere ausgewählten Experten vermitteln wichtiges Wissen und geben Ihnen ein Update in einer Webcast-Sendung. Buchen Sie die ganze Webcast-Reihe oder einzelne "Essentials": So erhalten Sie einen aktuellen Überblick und erweitern Ihre Komptenzen.
Il nostro seminario intende trasmettere ai partecipanti il know-how necessario per poter importare e distribuire correttamente un Dispositivo Medico/IVD partendo dai requisiti normativi cui ottemperare, dai compiti e dalle responsabilità previsti a tal fine e con particolare riguardo alle relazioni con il fabbricante.
All the essentials of clinical trials in Europe in only two days! Six experts will share their in-depth knowledge with you to introduce you as beginner or update you as professional on the most important aspects. Pose your individual questions in advance or live to make the most of your training!
Learn the essentials of the MDR and how to navigate around the legislation and to apply it.
Participants, doing business in a complex multi-jurisdictional environment, will be enabled to address difficult situations when designing and negotiating IP related agreements in cross-border projects.
Participants, doing business in a complex multi-jurisdictional environment, will be enabled to address difficult situations when designing and negotiating IP related agreements in cross-border projects.
