Rare Disease & Orphan Drug Development - Cost-efficient trial design to minimise cash burn
Discussion topics include: Key challenges to improve cost-efficiency in clinical development of orphan drugs Regulatory evolution in the review process…
Webinars
Discover the latest in clinical development, trials and data management, from our in-house experts, available on demand now.
Phase I Studies in Patient Populations:De-risking Clinical Development by Obtaining Key Patient Data Earlier
In this webinar members of our specialist, early phase Project Management team will discuss how they tackled the range of challenges faced to successfully execute a variety of Phase I clinical studies in patient populations.
Effective Implementation of the Revised EMA First-into-Human (FiH) Guidance to Accelerate Your Early Clinical Development
Available to view on demand. In this webinar the speakers discuss the use of integrated protocols (umbrella protocols) to maximise programme…
Scintigraphy: Providing Critical Data in Early Clinical Development
Available to view on demand. If you are embarking on your clinical development plan, consider a non-invasive in vivo evaluation of drug…
Conducting Early Phase Oncology Studies - Successfully moving through to proof of concept and beyond
Available to view on demand. This one-hour webinar focuses on strategic considerations for the molecule, including a brief review of the…
Agility In Rare Diseases & Oncology Clinical Trials - Data Management
Available to view on demand. Modular and adaptive clinical trials are rapidly expanding the ability of researchers to modify clinical…
Achieving Orphan Designation (ODD) - Meeting the unmet need
Available to view on demand. Achieving Orphan Drug Designation is a significant step enabling your product to be licensed faster, in a cost-efficient…
ESMO Update: State of the Art in Early Phase Oncology Trial Design
If you missed our live ESMO Update: State of the Art in Early Phase Oncology Trial Design webinar you can…