I architect auditable decision systems

for FemTech & regulated health platforms

Biology, software, and regulation must agree — or products fail.

I work with:

  • CTOs and platform leads building regulated health or FemTech products
  • Founders preparing for audits, clinical validation, or regulated expansion
  • Product teams scaling clinical logic into software

Most health platforms fail because the decision logic is:

  • Not traceable
  • Not biologically and biochemically aligned
  • Not audit-ready

Instead, I turn implicit clinical reasoning into explicit, verifiable system logic.

This is where clinical judgment must be translated into explicit, verifiable system logic.

My work combines:

1. Biological systems intelligence: Functional medicine, metabolism, women’s health complexity
2. Regulatory & quality logic: Pharma 4.0, batch release thinking, compliance-first architectures
3. Systems translation: Turning clinical judgment into software-safe, auditable logic.

I do not offer generic consulting.

I embed decision frameworks into products.

Credentials & Applied Experience

Education

– Ms in Medical Biophysics
– MRes in Nutrition and Metabolic Disorders
– Certified in Functional Medicine
– Certified in Pharma Quality Leadership (through HGA, Germany)

Experience

– Designed 4 women’s health programs used in clinical practice
– Authored a 100,000-copy book on endometriosis-related pain
– Built functional protocols for hormonally complex patients
– Designed a solution for a CDMO Batch Release Regulatory Bottleneck