EU IVDR Application Countdown
Brexit regulatory
environment
Brexit regulatory
environment
Services
Comprehensive service offerings at every point in the product life cycle.
Medical Device QMS
Risk Management
In-Country Representation
Regulatory Strategy
Technical File and Dossier Development
Post Market Surveillance
Software Compliance
Business Support
AI & ML Regulatory Compliance
With more than 5 years experience in Software as Medical Device Compliance and successful running clients in Artificial Intelligence and Machine Learning in MedTech industries, Rico solutions is specialised in AI&ML Regulatory compliance.
Let us together build a flourishing business
Using our Business Support Services, Rico solutions enables customers to operate a lean, agile business without losing opportunity. By combining our expertise, technology, and industry knowledge, Rico solutions allows you to focus on what you do best—designing, commercializing, or sourcing of innovative medical and health-tech devices—while we anticipate and respond quickly to your regulatory needs.
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Countdown to EU IVDR
In Vitro Diagnostic manufacturers in the European marketplace need to develop and implement strategies in order to be fully compliant. They will otherwise face resource challenges if preparation is left to the end of the transition period.
Date of application to the EU IVDR
26th May 2022
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