Thursday, October 6, 2016

Preparedness and Collaboration as a Response to Global Health Epidemics

Global-Health-World-Stethescope

By, April Schultz, Content Marketing Writer, Forte Research Systems

Epidemics are the stuff of nightmares. Particularly in the clinical research field, epidemics pose many challenges, often requiring rapid action, immediate trial start-up, and low-standard good clinical practice (GCP), among other struggles. Ultimately, it’s incredibly difficult to conduct a clinical trial during the course of an epidemic. Ebola and Zika are two recent (and current) global health concerns that serve to illustrate these challenges, and continue to test researchers.

However bleak this may seem, such challenges can be overcome. On day two of Partnerships in Clinical Trials US, two inspiring presenters shared their journeys working to combat infectious diseases, such as Ebola and Zika, in Third World countries. Both presenters asserted the common idea that the research industry needs to work together to become more prepared for epidemic response before an outbreak occurs.
Data-driven preparedness 

Presenting in the large Exhibit Hall, Toni Hoover of the Bill & Melinda Gates Foundation spoke on the power of technology and therapeutic innovations to fight diseases that afflict underprivileged individuals. She stated that the Bill & Melinda Gates Foundation, an organization dedicated to improving quality of life around the world, works with many partners to provide vaccines and novel therapies to individuals in impoverished communities.

The Foundation and its partners in the biotech space are working to collect data necessary to make informed decisions in the event of an epidemic. Hoover celebrated the potential for this data to be used to predict where the next epidemic may occur, declaring that the whole healthcare ecosystem needs to work together to prepare and develop a platform for dealing with epidemics such as Ebola and Zika. She noted, “Zika is an example of how we need to think about interventions, but also how we can be prepared by collecting the right data to inform decisions.”

Industry transparency 

Similarly, presenter Trudie Lang of the Global Health Network at the University of Oxford asserted her belief that the clinical research industry needs to be more prepared to respond in the event of an outbreak.

Lang shared her experience as a researcher conducting an Ebola trial in West Africa. She described the rush to begin the study and the immense pressure to complete the trial in only 16 weeks. Though her team managed to set up and complete the clinical trial at lightning speed, Lang admitted, “We were too late. The epidemic was already on the downward slope by trial completion.”

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This experience proved to Lang that the research community must be ready to respond to infectious diseases before an epidemic reaches this downward slope, and possibly before an outbreak occurs. “Research cannot be an afterthought [in the event of an outbreak]; it should be embedded in the initial response” she stated.

Lang went on to propose a solution: shared research information and transparency in the clinical research industry. She stressed that the same issues plague every clinical trial, namely patient recruitment, study compliance, and more. Lang argued that sharing clinical research information between groups, disease areas and regions would make research more agile, allowing quicker response to life-threatening diseases.

While epidemics and global illnesses are incredible cases of the need for organizational collaboration and information sharing, these ideas are also applicable on a smaller scale. These two presenters revealed that a more communicative, collaborative research industry could change the conduct of clinical research for the better and lead to greater efficiencies for potentially life-changing clinical trials.

April Schultz is the Content Marketing Writer at Forte Research Systems, a developer of clinical research software. In this role, she is responsible for the creation and direction of Forte’s educational materials such as blog articles, eBooks and webinars. She manages Forte’s content calendar, oversees content posted to the Forte Clinical Research Blog (http://forteresearch.com/news/) and works with presenters to host Forte’s monthly educational webinar series.




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