Discover the latest in clinical development, trials and clinical data management, from our in-house experts. Available on demand, now. Why not also explore our clinical white papers for even more information?
Now available on demand Being first to market with an innovator drug remains the ultimate goal for all and most organisations are constantly reviewing timelines in order to achieve efficiencies through trial design, conduct and the reduction of down time between phases of their drug development. As a small biotech,…
Clinical trials for central nervous system (CNS) conditions have historically been notoriously difficult for a myriad of reasons with a failure rate…
Decentralisation has been one of the biggest outcomes of the COVID-19 pandemic. The speed and degree to which traditional healthcare…
Genomic sequencing techniques and bioinformatics have led us to a better understanding of cancer biology, resulting in a shift from…
In early clinical development, making changes to a study design after regulatory approval can cause significant delays. These can be avoided…
A Discussion on Regulatory and Operational Considerations This 1-hour webinar discusses how the COVID-19 pandemic has impacted clinical studies for…
This 1-hour webinar reviews a published consensus statement from the British Journal of Cancer (BJC), looking at recommendations for effective…
In this webinar members of our specialist, early phase Project Management team discuss how they tackled the range of challenges…
Discussion topics include: Key challenges to improve cost-efficiency in clinical development of orphan drugs Regulatory evolution in the review process…
In this webinar the speakers discuss the use of integrated protocols (umbrella protocols) to maximise programme efficiency. Attendees will learn how…
If you are embarking on your clinical development plan, consider a non-invasive in vivo evaluation of drug delivery systems. Scintigraphy gives you the…
Early phase oncology trials are the first stage in testing new cancer treatments. This usually encompasses phase I and phase…
Achieving Orphan Drug Designation is a significant step enabling your product to be licensed faster, in a cost-efficient manner, and achieve market exclusivity…