Business Planning service
MedTech Market Readiness: Integrated Regulatory Compliance & Investor-Grade Clinical Strategy
Provided by Munich MedTech (a brand of AR2-C2 GmbH) · Germany
Service description
This service provides a comprehensive Regulatory & Clinical Strategy Roadmap designed specifically for HealthTech startups targeting the European market. Unlike standard compliance support, we integrate EU MDR/IVDR requirements with your commercial milestones to ensure investor readiness. Key Deliverables: Regulatory Gap Analysis & Classification Report: A clear assessment of your device under MDR 2017/745 or IVDR 2017/746. Clinical Evaluation Strategy: A step-by-step plan for generating the clinical evidence required for CE marking and reimbursement. Technical Documentation Structuring: Guidance on building a compliant Technical File ready for Notified Body submission. Investor-Ready Risk Assessment: Identifying regulatory risks that could impact valuation and fundraising. This service bridges the gap between technical compliance and business growth, reducing your time-to-market and de-risking your path to Series A/B funding.