Quick approval for your medical product

HERE WE INTRODUCE OUR COMPETENT EMPLOYEES

To reach any of our staff members, please contact our headquarters (telephone +49 (0)89.45 20 676-0 | email info@regular-services.com) or visit our Contacts page for the individual email adresses.

 

Hans-Peter Wettl

Managing Director
and Founder
Senior Consultant

Master Degree Electrical Engineering

Area of expertise
CE marking, Quality Management (ISO 13485, 21CFR820), 510(k)-Clearance, European Directives, European Guidance Documents and Standards, Author of Feature Publications in all areas of European Medical Device Regulations

 

 

Robert Karl Ibler

Managing Director

Senior Consultant

Robert Ibler

Master Degree Physical Engineering

Area of expertise

CE marking, Quality Management
(ISO 13485, 21CFR820), European Directives,
European Guidance Documents and Standards,
Author of Feature Publications in all areas of European Medical Device Regulations

 

Dr. Michael Dörffel

Senior Consultant

Master of Science in Physics

Area of expertise
CE marking, Quality Management (ISO 13485, 21CFR820, Ordinance 169), 510(k)-Clearance, European Directives, European Guidance Documents and Standards, Author of Feature Publications in all areas of European Medical Device Regulations

 

 

Alexander Popp

Senior Consultant

Master Degree in Mechanical Engineering

Area of expertise
CE marking, Quality Management (ISO 13485, 21CFR820, Ordinance 169), European Directives, European Guidance Documents and Standards Regulatory specialist EEA, USA, South America, Australia, Asia

 

 

 

Kerstin Klein

Senior Consultant

Master Degree in Biomedical Engineering

Area of expertise
CE marking, Quality Management (ISO 13485, 21CFR820, Ordinance 169), European Directives, European Guidance Documents and Standards, Clinical Evaluation, Regulatory Specialist EEA, USA, Japan, Australia, Middle East, Asia

 

 

 

Anika Reibenspiess

Consultant

Master Degree in Biomedical Engineering

Area of expertise
CE marking, Quality Management (ISO 13485, 21CF820), Biological safety, Clinical Evaluation, Electrical basic safety and essential performance, Usability, RoHS II

 

 

 

 

Andreas Esch-Brödner

QM Documentation Specialist and Assistant

Andreas Esch

Sales & Marketing

Area of expertise

Quality Management
(ISO 13485, 21CFR820), Technical Files for CE-marking, Customer Support

 

Gerhard Willberger

Consultant

Gerhard Willberger

Business Administration

Area of expertise

CE marking, Quality Management (ISO 13485, 21CFR820), Author of Feature Publications in all areas of European Medical Device Regulations, Translations, Power Point Presentations

 

 

Claudio Zuppa

Head of System Administration

 

 

 

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Claudio Zuppa

Mathematics

Area of expertise

IT


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