Client project – Richard Wolf
More than 30 Clinical Evaluations covering over 4,000 products and a partner who thinks ahead.
Dr. Monika Häfner, Head of Clinical Affairs:
We have been working with Regular Services since 2021 – originally looking for an external partner who can truly match our level of expertise.
The MDR transition presented our portfolio with a clear task: systematically revise more than 30 Clinical Evaluations, keep them up to date, and ensure they are regulatory-compliant. For that, you need someone you can speak to directly — without translation effort, without the feeling of having to explain what you need. Sometimes Regular Services already knows before you have finished your own train of thought.
What sets the collaboration with Regular Services apart: you can tell there is genuine expertise behind it – including in dealing with Notified Bodies. We can discuss regulatory questions directly, weigh options together, and make decisions. When priorities shift or projects are swapped, it is simply implemented.
What I particularly value: Regular Services does not only look at what is immediately at hand – but also at what is coming next.
“What we value about Regular Services: it is not a project that gets delivered. It is continuous support — and that makes the difference.”
Dr. Monika Häfner, Head of Clinical Affairs
Are you looking for a partner, not just a service provider?
Just as we do with Richard Wolf, we work with many manufacturers on a long-term basis — in clinical and performance evaluation, as equals and over many years.
Schedule a free initial consultationOur services
From the initial regulatory assessment to ongoing market support – all from a single source.
Our customers
Medical Device
manufacturers
Start-ups
Suppliers for medical devices / IVD
Authorities
IVD manufacturers
Investors