IP strategy

White paper

IP strategy

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.


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Editor: Patentopolis B.V. 


 

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White paper

IP strategy

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Events for „IP“

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Qualification Course Regulatory Affairs Manager

With our modular qualification course, you can expand your competencies in drug regulatory affairs in a targeted and practice-oriented manner. You design your learning pathway individually and set professional focus areas in line with your occupational requirements. Including an overall certificate and up to 30% price advantage compared with individual bookings.

online 01/01 - 31/12/2026
e-Learning: GDP - Basic Training

This e-Learning programme will provide you with knowledge on Good Distribution Practice in today's pharmaceutical industry

online
e-Learning: AMNOG briefly and concisely

e-Learning in 5 modules: concept, data requirements and the AMNOG process up to the price negotiation

online
e-Learning: Refresher Medical Device Advisor §83 MPDG

Our e-learning, specially tailored for medical device advisors, provides you with the essential knowledge to navigate your professional duties confidently and in full legal compliance.

online
e-Learning: Medical Device Advisor §83 MPDG

Our e-learning, specially tailored for medical device advisors, provides you with the essential knowledge to navigate your professional duties confidently and in full legal compliance.

online
e-Learning: Introduction to EU Marketing Authorisation

This e-learning programme will familiarise you with the regulatory affairs principles involved in applying for a marketing authorisation in Europe (MRP, DCP, CP) . It will also introduce you to post-authorisation duties (renewal, variation...).

online
e-Learning: EU Variation System and Procedures

This e-Learning programme will provide you with detailed knowledge on the classification, grouping and submission of variations in the EU.

online
e-Learning: Common Technical Document and eCTD

Do you need know how regarding CTD/eCTD & CMC? Then this e-learning programme is the fast track to becoming knowledgeable in this field. No prior dossier experience is required.

online
IP Agreements: Research and Development Agreements

Participants, doing business in a complex multi-jurisdictional environment, will be enabled to address difficult situations when designing and negotiating R&D agreements in cross-border projects.

online 18/03/2026
IP Agreements: Patent License Agreements

Participants, doing business in a complex multi-jurisdictional environment, will be enabled to address difficult situations when designing and negotiating patent license agreements in cross-border projects.

online 19/03/2026
How to Protect And Manage Trade Secret Assets

This online course provides essential understanding of statutory and contractual trade secret protection especially against insider and outsider theft. The online course assists in the organization of statutory and contractual instruments and helps to understand their impact on corporate life.

online 19/03/2026