Join our one-day course and discover how to revolutionize your patent work with the power of generative AI. This immersive workshop offers patent attorneys, counsels, and engineers a unique opportunity to gain hands-on experience with generative AI.
Artificial intelligence is being hailed as the next key innovation. This course will show you how to integrate suitable systems and applications into your daily workflow and simplify business processes between your PV and IT departments using AI. Register now to stay ahead.
The purpose of this online course is to inform the participants how to prepare an international application for filing under the PCT and subsequently monitor the consecutive procedural steps, timelimits and payment of fees in the PCT international phase up to and including entry into the national phase in designated and elected states.
Interested in establishing a strong presence in the Chinese medical devices market? Join our training to gain valuable insights into the latest Chinese regulations governing medical devices, and discover strategies to optimize your pre-market registration and post-market surveillance. Benefit from the expertise of our local specialists, who will share up-to-date information to enhance your success
RNA-based drugs and oligonucleotides: gain a solid understanding of the complexities involved in the development and regulatory approval of RNA-based drugs and oligonucleotides. Meet outstanding and longtermin experienced experts in the field of research.
Struggling with the complexities of IT tools for EU and national funding programme implementation? Join our seminar to unlock the solutions you need. We'll guide you through tackling the challenges, ensuring your programmes run smoothly and efficiently.
During our online training "Toxicology and beyond: Safety assessment in drug development" you will build a solid toxicological know-how basis and will be informed about the inclusion of toxicological data in the marketing authorisation dossier. Take the chance and participate in our interactive online training.
Two successful EPAC 2022 participants will pass on their tips and tricks so that attendees for the EPAC will be well prepared. Integral part of the course is a real-time mock.
Wondering how to navigate the complexities of EU Fund audits? Regulation (EU) 2021/1060 consolidates rules for the ESI Funds, the Fisheries and Aquaculture Fund, the AMIF, the ISF, and the BMVI. While there may be nuances between these funds, the foundational principles of auditing remain consistent. Our seminar is designed to assist professionals embarking on their journey with these funds.
The most important decisions of the Boards of Appeal in the field of biopharmaceuticals and biotechnology and changes in the Guidelines will be presented. The panelists will discuss, in particular, the consequences of these decisions and changes on patent practice.
In the current programming period, Art. 18 of the Common Provisions Regulation (CPR) has introduced a few changes on performance-oriented programming for ERDF, ESF+, Cohesion Fund and JTF-supported programmes. Our two-day seminar offers an immersive and practical training for the Funds implementation.
