Transforming complex clinical knowledge into structured, actionable frameworks for research, clinical decision support, and HealthTech platforms.
My work supports academic teams, FemTech and HealthTech innovators, and digital therapeutics developers, bridging evidence, clinical workflows, and systems thinking.
Clinical Knowledge Architecture
Design and structure of clinical frameworks that make complex health knowledge explicit, navigable, and referable.


Wearables

Evidence Structuring & Integration
Synthesis of scientific literature into usable frameworks, evidence maps, and concept taxonomies.




Clinical Decision Support Foundations
Early-stage conceptual support for CDS systems, including:
- Evidence models
- Scope definitions
- Pattern frameworks and heuristics
(Note: this is foundational and research-oriented; not live software.)
HealthTech Content Enablement
Preparation of clinical knowledge artifacts for:
- AI interpretation
- Tool integration
- Research annotation
Translations

FAQs: Why Work With Me?
1. What makes your HealthTech content services unique?
I bring 20 years of healthcare experience across clinical pharmacy, the NHS, medicines regulation, and digital health. My expertise lies in structuring complex clinical knowledge, evidence frameworks, and decision-support content for SaMD, FemTech, and AI-driven platforms. I translate intricate workflows into clear, usable content that supports clinicians, researchers, and digital health innovators.
2. How does your HealthTech consultancy support my project?
I focus on content architecture, knowledge structuring, and usability, not IT development. I advise on organising clinical content for regulatory compliance, clinician adoption, and evidence alignment, ensuring your platform’s content is accurate, structured, and ready for integration into digital health tools.
3. Why choose you over other HealthTech content providers?
My background combines clinical pharmacy, regulatory expertise, and digital health experience, offering a rare perspective on bridging complex clinical workflows with structured, actionable content. I help teams create frameworks that are research-ready, CDS-ready, and aligned with modern multi-system health approaches.
4. How does your clinical pharmacy background benefit HealthTech clients?
It provides a deep understanding of clinical workflows, regulatory requirements, and patient-centered care, which informs the development of accurate, structured, and usable clinical content. This expertise ensures that content is suitable for decision-support systems, research tools, and digital therapeutics.
5. What experience do you have with SaMD, FemTech, and AI in Healthcare?
I have designed and structured clinical content for digital health platforms, including diagnostic tools, clinical decision support, and AI-informed applications. My work ensures content meets regulatory standards, is organised for usability, and integrates smoothly into HealthTech systems.
6. How does your MSc in Clinical PsychoNeuroImmunology add value?
My MSc provides a scientific, research-based understanding of multi-system health interactions, informing structured clinical content and knowledge frameworks. This expertise allows me to translate complex, integrative concepts into actionable content for HealthTech, CDS, and research applications.
7. What can I expect from working with you?
Expect a collaborative, research-informed partnership. I listen to your goals and deliver structured, evidence-based clinical content and consultancy tailored to your platform’s needs, whether for decision-support, regulatory compliance, or knowledge frameworks.
8. How do you ensure content aligns with my HealthTech goals?
I start by clarifying your platform’s objectives—research, clinician adoption, or system integration. Using my clinical, regulatory, and digital health expertise, I develop structured content strategies and frameworks that align with your goals. Regular feedback loops ensure your SaMD, FemTech, or AI tool receives content that is accurate, organized, and actionable.