Clinical trials represent a critical stage in drug development fraught with complexities and unpredictability. External consultants provide vital support through their expertise in navigating the intricate regulatory landscape and ensuring timely project execution. Rasmus Rabøl, a consultant from KLIFO, emphasizes the need for mutual trust between consultants and clients, highlighting how a thorough grasp of both scientific and regulatory aspects is essential for success. Trends such as the rise of smaller companies and the impact of AI tools are shaping the future of clinical research.
1. Drug development is unpredictable and resource-intensive. 2. Consultants offer strategic guidance to mitigate risks. 3. Trust is vital in consultant-client relationships. 4. AI tools are enhancing trial efficiency. 5. A rise in smaller companies is leading to more outsourcing. 6. Flexibility in planning is crucial for success. 7. Understanding regulatory landscapes is key for consultants. 8. Prioritizing biological understanding can reduce clinical trial attrition.
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