Register Now: Beyond EDC: Designing a Connected Data Strategy for Predictive Clinical Development
Logo Image
News|Webcasts|July 15, 2024

Patient Technology: Implement the Right Technology at the Right Time for Your Trial

Author(s)IQVIA

Webinar Date/Time: Tuesday, August 13th, 2024 at 11am EDT|8am PDT|4pm BST|5pm CEST

When sponsors invest in best-of-breed solutions that leverage intelligent integration and workflow automation, it is possible to support a positive technology experience for sites and optimize the clinical supply chain. In this webinar, IQVIA patient technology experts will dive into the flexibility you have when deciding what approach to take when implementing patient technology into your next trial.

Register Free: https://www.appliedclinicaltrialsonline.com/act/patient-technology
Event overview

To improve data quality, reduce site effort, optimize workflows in your clinical trials, and address problems at hand, you need the right technology at the right time. While an integrated platform approach might be best to tackle your goals, you may, instead, only need one or two point products.


When sponsors invest in best-of-breed solutions that leverage intelligent integration and workflow automation, it is possible to support a positive technology experience for sites and optimize the clinical supply chain.

In this webinar, IQVIA patient technology experts will dive into the flexibility you have when deciding what approach to take when implementing patient technology into your next trial.

Three key take-aways

  • Design and execute a patient technology strategy that fits your needs.
  • Reduce clinical site burden by streamlining processes across eConsent, IRT, and eCOA.
  • Quickly leverage insights collected from patient data to improve compliance, study optimization, and decision making.

Who Should Attend

  • Clinical Operations (all)
  • Clinical Development (all)
  • Patient Engagement
  • Therapeutic Area Leads
  • Therapeutic Expert
  • Procurement
  • Med Affairs
  • IT
  • Clinical IT

Speakers:

Anthony Mikulaschek
Vice President, Commercialization, IQVIA Patient Suite
IQVIA


As the vice president of commercialization for the Patient Suite at IQVIA, Anthony Mikulaschek is responsible for the commercialization of IQVIA's eCOA, eConsent, and IRT platforms. This includes pricing and sales strategies, opportunity configuration, market needs review, IQVIA technology market placement, and strategy. Anthony has extensive experience in validated system configuration, implementation, systems integration, business process reengineering, IT operations, and consulting. He has successfully led the development, delivery, and management of technology solutions for over 37 years. This includes 29 years of experience in the pharmaceutical sector.


Kevin Landells
Vice President, Delivery, IQVIA Patient Suite
IQVIA

Kevin has over 25 years of experience in the IRT/ RTSM industry, having worked across many technical and project management leadership roles. Experienced with developing and leading global teams that deliver managed services spanning operations, project management, client partnerships, and business transformation, Kevin is passionate about improving healthcare and utilizing technology that makes a real difference to patients’ lives. Kevin holds a bachelor’s degree in computer science from Hertfordshire University.

Register Free: https://www.appliedclinicaltrialsonline.com/act/patient-technology

Related to this article

View more
What Needs to Happen Beyond the Clinical Trial Modernization Act
What Needs to Happen Beyond the Clinical Trial Modernization Act
In this video interview, Kent Thoelke, CEO of Paradigm Health, calls for safe harbor protections, CMS reimbursement safeguards, and funding mechanisms modeled on EHR meaningful use to help community and rural institutions participate in research on par with academic centers.
Read more
Building AI Assistants Clinical Trial Teams Can Trust: Q&A with E.K. Koh, Suvoda
Building AI Assistants Clinical Trial Teams Can Trust: Q&A with E.K. Koh, Suvoda
In this Q&A, E.K. Koh, chief product officer at Suvoda, discusses what separates a trustworthy AI assistant from one that adds risk, why curated clinical knowledge matters more than general-purpose flexibility, and what safeguards must be in place when assistants move from answering questions to taking actions in clinical trial systems.
Read more
© photon_photo - © photon_photo - stock.adobe.com
Building Standardized Evidence for eSource-Enabled Clinical Trials: Multi-Site Validation of a Clinical Research Coordinator Satisfaction Methodology
Standardized measurement across five oncology centers found that clinical research coordinators rated eSource-enabled workflows positively (Overall Mean Satisfaction 5.79 of 7), with reduced manual entry and electronic data transfer earning strong marks, while perceived reduction in sponsor and monitor queries lagged as the one domain below threshold.
Read more
Where the Industry Is Headed as Clinical, Operational, and Real-World Data Connect
Where the Industry Is Headed as Clinical, Operational, and Real-World Data Connect
In this video interview, Rajneesh Patil, global head of AI, digital, and innovation in clinical development at Syneos Health, describes the industry’s trajectory toward a unified intelligence orchestration environment—and explains why the future isn’t one model that knows everything, but a trusted system that brings the right evidence to the right human decision.
Read more