The EU's Recovery and Resilience Facility (RRF) is an essential part of the EU's economic recovery plan, providing grants and loans to member states. Since its launch in 2021, implementation has been uneven across EU countries. What are the reasons for these differences in implementation between EU countries, and how can one navigate the new system for successful RRF funding?
The conference offers you once again the most recent developments in IP for the seed industry and the breeders.
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.
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.
Get practical expertise for the GMP, GLP and GCP-compliant archiving of relevant documents and the efficient integration of the archiving system into your daily work processes. The three experts will show you some practical approaches to typical pitfalls.
FDA inspection readiness: Gain the knowledge and skills necessary to manage future FDA inspections with confidence and ease.
This online course aims at providing attendees with the mindset, the methodology and the tools to move a traditional IP department to an agile IP department.
Do you already have a good understanding of PSUR and RMP including risk minimisation measures and would like to deepen, broaden and update your knowledge? Then this course is for you! Learn about pharmacovigilance requirements in the drug lifecycle and their impact on RMP and PSUR from a global perspective. Save your place now!
Are you new to pharmacovigilance and looking to kick-start your career? Then this online course is just for you. Gain a comprehensive overview of pharmacovigilance, regulatory requirements in the EU and implementation in only two days. Book now!
Do you want to independently plan and conduct pharmacovigilance audits? Then take this opportunity to become an "Auditor for Good Pharmacovigilance Practices". Secure your place on our compact, interactive online course. Book now!
With our e-learning specially tailored to medical device consultants, you will receive the knowledge essential for medical device advisors - so that you can move about in your everyday professional life with legal certainty!
