Maximal Challenges, Opportunities, and the Evolving Role of IP Professionals
Artificial intelligence and machine learning are reshaping the field of intellectual property. This white paper presents expert insights on patenting AI/ML inventions, integrating AI into IP workflows, and the changing role of IP professionals.
Edited by Jean-Claude Alexandre Ho LL.M., the white paper is based on interviews with leading IP experts and was summarized using NotebookLM.
Combined offer of three compulsory seminars plus one elective module for (future) Heads of the Pharmacovigilance Department - learn the responsibilities and legal aspects of managing a PV system and its staff, and select an elective module according to your individual interests.
Combination of three selected seminars - with this qualification course, you will first gain insight into the legal aspects and general responsibilities of the Qualified Person for Pharmacovigilance (QPPV). You will then deepen your professional and practical knowledge to perform your role more effectively.
This e-Learning programme will provide you with knowledge on Good Distribution Practice in today's pharmaceutical industry
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.
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.
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...).
This seminar offers beginners in clinical project management the opportunity to gain comprehensive insight into their responsibilities as clinical project managers and to acquire both specialized project management knowledge and skills in team leadership and communication.
CMC dossier requirements FDA vs EU: After having attended the seminar you will feel secure writing and maintaining the quality dossier for US marketing authorisations of small and large molecules (chemicals and biologic).
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.
Our speakers will suggest authoritative answers to key problems of EU design law and give an update on most recent case-law
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.
