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.
- Registration possible until 17.02.26 - This two-day online course strengthens your skills in writing key pharmacovigilance safety documents. You will gain a clear understanding of regulatory requirements and hands-on experience in drafting and maintaining DSURs, PSURs and RMPs.
Gain a thorough understanding of the latest accounting standards for national and international banks through detailed examples, all available online.
This online seminar provides a comprehensive overview of global regulatory affairs, covering strategies for setting regulatory policies, developing global regulatory dossiers, understanding HTA interfaces, enhancing global communication, and staying updated on ICH guidelines, ISO IDMP updates, and global regulatory trends.
