Let's Connect the Dots to Make Lives Better
What I do
Thoughtful, Intentional, & Efficient
As we move from reactive thinking to proactive, evidence-driven approaches in drug and device development, the focus must shift toward human-centered, evidence-driven approaches. Anticipating needs early enables solutions that drive meaningful impact, adoption, and better patient outcomes.
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Meaningful Measurements
After 8 years of designing trials that actually reflect patient lives, clinging to either active or passive COAs is a losing strategy—and blending both can slash trial failures while putting patients first.
Integrated Evidence
It is a continuous approach to generating and collecting data throughout the lifecycle of a medical product or intervention for a more holistic, accurate, and comprehensive foundation for decision-making.
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Regulatory Roadmap
The roadmap provides a simplified and visual representation of the path for approval, helps manufacturers roughly estimate the effort required to meet the requirements, and shows the responsibilities for the individual process steps.
Integration with
the Eco-system
The implementation of evidence is often considered time-critical but requires careful planning for the core integration within the lifecycle and this underlines the point that co-creation with the ecosystem is a "must" for impactful innovation.
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