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Scintigraphy: Providing Critical Data in Early Clinical Development
19/06/2019
If you are embarking on your clinical development plan, consider a non-invasive in vivo evaluation of drug delivery systems. Scintigraphy gives you the power to study drugs in gastrointestinal organs, providing you with valuable data earlier on in the drug development process. In this webinar, our featured speakers cover:
Achieving Orphan Designation (ODD) – Meeting the unmet need
26/04/2018
Achieving Orphan Drug Designation is a significant step enabling your product to be licensed faster, in a cost-efficient manner, and achieve market exclusivity for 10 years. Watch this 1-hour on-demand webinar where you will gain a practical overview of the steps to achieve orphan status including: For more information on rare diseases, take a look at our rare […]
Conducting early phase oncology clinical trials: key considerations
05/12/2017
Early-phase oncology trials are the first stage in testing new cancer treatments. This usually encompasses phase I and phase II of the three main phases of clinical trials, where patients are amongst the first to test a new treatment. Early-phase oncology trials generally test gradually increased dosage levels of an experimental drug. The toxicity and […]
Rare Disease & Orphan Drug Development – Cost-efficient trial design to minimise cash burn
01/06/2017
Discussion topics include: Despite the benefits of orphan drug development, cash burn minimization is one of the major challenges faced by developers. While guidelines exist for efficient orphan drug development, they should be adapted to challenges presented by each of the more than 7,000 recognized rare diseases. The clinical development of orphan drugs represents a […]

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