Regulatory processes must become smarter.
Higher requirements do not simply mean a higher headcount.
My passion is the digitalization of RA, QA and R&D.
As a result, development, placing on the market and post market surveillance are becoming more cost-effective and even better.
1. Lower your costs
2. Gain your compliance
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My passion
MDR Implementation
EU Medical Device Regulation Implementation Roadmap and a smart approach.
Technical Documentation
Lean documentation according MDR and MDD.
Digitalization
Lower costs and gain compliance.
Digitalizing RA, QA and R&D.
Medical Device Content Management
With the manufacturer in mind to challenge the EU-MDR.
Digitalize your technical documentation!