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.
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...).
Join us for a free 1-hour webcast with the speakers of our upcoming EPAC 2025 seminar. Get first-hand insights from professionals who have successfully passed the exam. Learn how they prepared, what worked, and what they'd do differently.
This topical in-person conference is about the latest developments in artificial intelligence and intellectual property. Attendees will get insights into the 'hot' topics of this super trend from top speakers from the industry and private practice.
Master the art of successful business negotiations with expert guidance from international negotiation trainer Frans Schram. This interactive online seminar equips professionals with proven strategies, persuasive techniques, and psychological insights to enhance negotiation skills.
Join our two-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.
In this hands-on seminar, you will discover the unique working methods and communication styles of Asian cultures to improve your intercultural skills and build stronger connections with your Asian business partners!
Master the logic of the EPAC exam questions through hands-on mock trials with the help of IP experts! Increase your chances for success on 9 October!
Are you a specialist in the pharmaceutical industry in the area of marketing authorization and responsible for compiling the quality documentation of active pharmaceutical ingredients (APIs) and their starting material? Then this is the right online seminar for you!
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.
