Regulatory, clinical and business due dilligence

MD101

France

Service ID:

EP212S3
Service description

The medical device sector requires a rigorous and precise assessment to ensure the viability and profitability of investments. MD101 offers specialised due diligence services, covering all critical aspects: a) Corporate governance; b) Business strategy; c) Clinical strategy; d) IT/cyber due diligence; e) US/EU regulatory strategy. Our services are designed to provide a comprehensive analysis (report) that helps entrepreneurs make informed decisions. This service is designed to help build a roadmap at all critical levels of a given project in the medical devices sector. The typical duration for this service is 6 to 8 weeks.

Sector
Healthtech
Medical Devices
Medtech
Technology Readiness Level
TRL 4 – Technology validated in lab
TRL 5 – Technology validated in relevant environment
TRL 6 – Technology demonstrated in relevant environment
TRL 7 – System prototype demonstration in operational environment
TRL 8 – System complete and qualified
TRL 9 – Actual system proven in operational environment
Financial requirements

Regulatory due diligence: 3 to 10-day assignment depending on the number of devices and markets to address at €210/ hour. 
Clinical due diligence: 5-day assignment at €312/hour. 
Business due diligence: 5-day assignment at €250/hour.

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