Medical strategies, built on the full picture.

    We map rare disease ecosystems and build living evidence systems that help biotech and pharma teams make better decisions across development, medical affairs, launch and market access.

    Our purpose

    From scattered evidence to better decisions.

    Entire ecosystem

    Not just KOLs.

    Clinicians, patients, treatment centres, payers and companies shaping the disease.

    Broader coverage

    Thousands of sources, gaps made clear.

    Evidence across countries and source types, with thin areas named.

    Kept current

    A living evidence base, not a report that ages.

    Refreshed as programmes, guidelines, competitors and markets change.

    Expert-reviewed

    AI expands the search, specialists validate it.

    Claims stay linked to sources and key readings are reviewed by people.

    How we work

    Build the evidence once. Use it for every decision that follows.

    One structured evidence base per disease. Not a new project for every question.

    1. 01

      Map the disease

    2. 02

      Validate the evidence

    3. 03

      Add the people and system

    4. 04

      Apply it to the decision

    5. 05

      Keep it current

    Decisions it supports

    • Indication choice
    • Trial and site strategy
    • Country prioritisation
    • KOL and centre mapping
    • Evidence gaps
    • Launch readiness
    Explore our services
    Team

    Built by people from rare disease.

    Our founding team pairs deep rare disease expertise with entrepreneurial execution and AI capability. Between us, we have worked across medical affairs, commercial strategy, scientific advisory, and AI-enabled innovation in metabolic disorders, neurological diseases, and oncology.

    Hilde Gerris Krol

    Hilde Gerris Krol

    PARTNERPhD Medical Biology
    • Deep industry experience in rare disease and specialty pharma
    • Medical Manager Benelux at Amicus Therapeutics
    • Background in medical community engagement and MSL leadership
    Jochem Bossenbroek

    Jochem Bossenbroek

    PARTNERMBA
    • Co-founded and Partner of a life sciences consultancy
    • Former CEO of a biotech company in infectious disease; from concept to clinical
    • Founder of digital nutrition care platform
    Patrick de Boer

    Patrick de Boer

    ADVISOR
    • Co-founder and Partner of a life-sciences consultancy
    • Founder of AI-powered pathology company for biopharma and clinical oncology
    • Founder of medical diagnostics company in infectious diseases

    Why Systemix

    Specialist research for the decision ahead.

    Rare disease decisions depend on understanding how the whole system works.

    Rare disease is all we do

    Small populations, uncertain evidence and complex care are our everyday work.

    Verified by the people who shape care

    We test key findings with clinicians, payers, labs, centres and patients.

    Europe, country by country

    Diagnosis, access and care differ by country. We analyse each market, not EU averages.

    A living picture, delivered by senior people

    AI widens the search. Senior partners interpret it and work with you directly.

    An example of the depth

    1,000+

    publications screened

    289

    sources across 89 organisations

    458

    traceable claims

    15

    expert interviews

    6 weeks

    to a pre-final landscape

    Illustrative figures from a recent European Batten disease landscape.

    See client results

    How clients can work with us

    Start with the decision. Build an evidence base that lasts beyond it.

    Intelligence starting point

    Consulting

    Focused research around one strategic decision. Delivered in weeks.

    • Rare disease landscaping
    • TPP validation
    • Barrier and driver analysis
    • Country prioritisation

    Ongoing intelligence

    Living Intelligence

    The evidence base stays current after the project. We track what changes and refresh the picture.

    • Therapy and diagnostic monitoring
    • New clinical evidence
    • Guideline and regulatory changes
    • Competitive intelligence

    Auditable by design

    Every finding stays linked to its source and version.

    Example claim record

    Claim
    “From 13 January 2028, EU joint clinical assessments also apply to orphan medicinal products.”
    Checked
    2 November 2026
    Version
    1
    Confidence
    High (legal text)

    Example for illustration. Every claim in a client deliverable carries these fields.

    Bring us in early.

    Tell us about the therapy, diagnostic or disease area you want to bring to patients. We will help you understand where the evidence is strong, where the gaps are and what you need to know next.

    Discuss your research needs