Author: Dr Anika Schröter
The development of RNA-based drugs has increased within the past years and is a promising field of research in the pharmaceutical industry. It is transforming the industry and will offer new hope for patients with unmet medical needs.
RNA-based drugs have several advantages over conventional drugs, such as the ability to target previously undruggable pathways, the rapid and cost-effective development, and the potential for personalized medicine. However, RNA-based drugs also face some challenges, such as the stability, delivery, and safety of the RNA molecules.
This whitepaper informs about the challenges with the 'standard' non-clinical program for different RNA-based drugs, focusing on safety evaluation.
Download now the white paper 'Non-clinical aspects of RNA-based drug development'.
We hope you enjoy reading it!
The conference will cover recent updates and practical implications of the EU pharmaceutical legislation, management of supply shortages, and the new EU Variation regulation. Additionally, it will address the latest developments in quality guidelines, impurities (with a focus on nitrosamines), and the application of AI in CMC and quality processes.
IP Strategy! - the interactive online course which helps you setting up convincing IP strategy plans.
The course "Aligning IP with Business Growth" is an in-depth course for helping you (re)align IP with the business. This course is not an extensive lecture about theoretical concepts. Instead, the course is 100% based on insights gained from actual practice; it provides tools, dashboards and empirical thinking directly applicable by the participants.
The seminar covers essential topics such as stakeholder identification, effective meeting preparation, and legally compliant collaboration. Tailored for Medical Science Liaisons (MSLs) and Medical Affairs teams, the seminar equips you to gain real insights from KOLs, overcome challenging situations, and elevate patient outcomes.
This online seminar provides knowledge on how to best reduce IP risks in R&D collaborations through contract design and management.
Gain a thorough understanding of the latest accounting standards for national and international banks through detailed examples, all available online.
This online course offers an in-depth overview of the medical device approval process in key global markets: Regulatory strategies, approval steps and timelines for global market access, with a focus on North and South America, the Asia-Pacific region and China.
Our experienced speakers will help you prepare for all the challenges facing board members in German banks.
Our experienced speakers will help you prepare for all the challenges that supervisory boards face.
Our speakers will give you tips and tricks on EP claim drafting and will show you which pitfalls to avoid.
Familiarize yourself with and explore the basic regulatory requirements and certification audit guidelines for auditing EU agricultural funds expenditures in the 2023-2027 programming period.
