Ledidi Partners
Find a Ledidi partner
From first study to post-market evidence, our partners bring the regulatory, clinical and data expertise to plan it, run it and prove it. Ledidi provides the platform, you keep the data, and together we help innovators bring compliant evidence to patients faster.
Clearpath Healthtech
United Kingdom • Europe
Regulatory, clinical and commercial consultancy for medtech, founded by ex-Notified Body, Big 4 and industry leaders.
Regulatory & Quality
Health Economics & Market Access
Clinical Evidence & Study Design
Post-Market Surveillance & PMCF
Digital Health & SaMD
Revolve Healthcare
Poland • Europe
ISO 13485-certified medical software development and regulatory consultancy, taking digital health products from concept to CE mark.
Digital Health & SaMD
Regulatory & Quality
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Mantra Systems
United Kingdom • Europe
UK medical device regulatory consultancy specialising in MDR/IVDR market access, clinical evaluation, SaMD and PMCF.
Regulatory & Quality
Clinical Evidence & Study Design
Post-Market Surveillance & PMCF
Digital Health & SaMD
NordicRWE
Norway • Europe
Real-world evidence company turning Nordic registry and health data into decision-ready evidence for pharma and biotech.
Real-World Evidence & Registries
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MedQtech (MedQdoc)
Sweden • Nordics (Denmark, Sweden, Norway) • Europe
Validated cloud eQMS for medical device companies, with 160+ templates mapped to ISO 13485, MDR/IVDR and FDA QMSR.
Regulatory & Quality
Franklyn Health
United Kingdom • Spain • Europe
Full-service CRO built for small and mid-size medical device and diagnostics manufacturers, from study design through to post-market follow-up.
Clinical Evidence & Study Design
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