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Cloud-based technologies based on years of proven best practices enable pharma sponsors and CROs to use secure single sign-on, make evidence-based decisions, and reduce clinical study startup time by at least 20%

DrugDev will demonstrate innovative clinical operations technologies aimed at promoting standardization, industry-wide collaboration, and a beautiful technology experience at the Clinical Innovations Congress in London, 9-10 March:

How One (Golden) Number Can Transform Clinical Trials, 9 March, 4:30pm – DrugDev’s Associate Director Bryan Dobson will discuss the impact of the DrugDev Golden Number – a unique identifier used to match and master Investigator and site information – on speeding site activation.  With the DrugDev Golden Number individual pharma companies and CROs easily match and master data, and share data across collaborations like the Investigator Databank and TransCelerate. Join this session for an update on the Golden Number and how pharma is using it to improve the efficiency of clinical trials.

The DrugDev Site Activation Module, 9 March 5:10 pm – At the Congress Tech Showcase Kirsty Kwiatkowski, Director, SiteStart will demonstrate DrugDev’s  new SaaS-based Site Activation Module, which will drastically reduce clinical trial startup time and ease the administrative burden on sites.  The Site Activation Module is a cloud-based technology that is driven by a customizable workflow optimization engine that simplifies e-feasibility, contract and budget negotiations, and the collection and maintenance of essential site regulatory documents. Productivity and collaboration are increased with global transparency, real time dashboards, metrics and reporting and more to reduce startup time by at least 20%.

About the Presenters

Bryan Dobson, Associate Director, DrugDev – Bryan has direct line management of Research Associates at DrugDev, and is responsible for data management and curation of the DrugDev Golden Number.  Prior to DrugDev Bryan was a Research Scientist in the Defence Technology Agency of the New Zealand Defence Force.

Kirsty Kwiatkowski, Director, SiteStart – Kirsty oversees SiteStart activities and the DrugDev Investigator Network. Kirsty is passionate about clinical research and the evolution of the clinical trials process and has many years of clinical and regulatory operations experience.  Previously Kirsty managed clinical trials and teams of clinical trialists at Vernalis, Johnson & Johnson and Pharm-Olam, where she worked across all phases of clinical research and several therapeutic areas.

Read what top pharmaceutical industry publications say about the DrugDev Site Activation Module:

Learn more about the Clinical Innovation Congress here: