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eCOA IRT eConsent: Simplifying User Experience and Driving Process Efficiencies Through Integration and Automation
This event is now available on demand.
Event overview
Implementing clinical technology strategies that improve data quality, reduce site effort, and optimize workflows is more important than ever. In addition, with the sharp rise in investigational product (IP) and shipping costs, it is crucial to take an integrated platform approach including advanced drug supply tools that optimize trial supply and support sustainability goals.
When sponsors invest in best of breed solutions that leverage intelligent integration and workflow automation, it is possible to support both a positive technology experience for sites as well as the optimization of the clinical supply chain.
In this webinar, IQVIA experts will share how to utilize integration and automation strategies to maximize trial efficiencies, reduce costs, and align with sustainability goals.
Three key take-aways
We’ll discuss how to:
Design and execute a clinical technology integration strategy that eliminates redundant activities such as duplicative data entry
Reduce clinical site burden by streamlining processes across eConsent, IRT and eCOA
Leverage insights from patient data quickly to improve compliance, study optimization and decision-making
For any technical questions please contact Jordan Ramesh:
jramesh@mjhlifesciences.com
Anthony Mikulaschek
Vice President, eCOA Operations
IQVIA
As vice president of eCOA operations at IQVIA,
Anthony Mikulaschek
manages all operations, data management, quality management, training and eCOA project work associated with IQVIA eCOA. Anthony has extensive experience in validated system implementation, systems integration, business process reengineering, IT operations, and consulting. He has successfully led the development, delivery, and management of technology solutions for over 30 years including 26 years in the Pharmaceutical sector.
Sonia Fischer
Customer Integrations Manager, Patient Consent
IQVIA Technologies
Sonia Fischer
is a health information technology leader with a focus on data interoperability. With over 20 years of experience in healthcare technology, Sonia is now focused on bringing her knowledge of clinical sites and software systems to the clinical trials industry as the Customer Integrations Manager for Patient Consent at IQVIA. In this role, she collaborates with clients on interoperability initiatives focused on connecting systems in order to improve clinical workflow and the patient experience from the point of consent.
She can be reached on LinkedIn at:
www.linkedin.com/in/fischersonia
Evan Slotter
Associate Director of Product Management, Cenduit IRT, an IQVIA Business
IQVIA
Evan
has over 16 years’ experience in IRT system design, development, and operations management. He has focused on bringing standardized component libraries and end-to-end solutions to enable more robust and efficient operations for clinical trials. He brings more than 30 years of experience within eClinical technologies, pharmaceutical and Integrated Circuit industries.
In his current role, Evan is working on clinical trial technology solutions enabling decentralized clinical trials, direct to patient and harmonizing patient data capture in areas around IRT, eCOA and eConsent.
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