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.
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.
This e-Learning programme will provide you with knowledge on Good Distribution Practice in today's pharmaceutical industry
e-Learning in 5 modules: concept, data requirements and the AMNOG process up to the price negotiation
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 e-Learning programme will provide you with detailed knowledge on the classification, grouping and submission of variations in the EU.
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.
Three e-Learning programmes in one bundle: Get a solid foundation in EU marketing authorisation procedures, the EU variation system and the Common Technical Document (eCTD). Your fast track into EU Regulatory Affairs - at a special bundle price.
Join our one-day course and discover how to boost patent drafting with the local generative AI. This immersive workshop offers patent attorneys, counsels, and engineers a unique opportunity to gain hands-on experience with local generative AI with ensured data confidentiality.
Get your know-how on creating and maintaining quality data for biotech products in our online training. Including an outlook on the new (Draft) ICH Q1 and ICH M4Q(R2).
