For manufacturers, importers, distributors and suppliers
Expert guidance from product idea to market access.
Process and cleaning validation, equipment qualification.
Setting up and maintaining QM systems according to ISO 13485, ISO 9001 and ISO 14001.
Internal audits, supplier audits and preparation for certification and regulatory audits.
Medical devices, biocidal products
I am a biologist with a doctorate (Dr. rer. nat.) specialising in microbiology and biofilms, and hold a Master's degree in Life Sciences (University of Konstanz). Building on many years of experience in antimicrobial materials, biofilms and biochemistry, I have been working since 2019 at the interfaces between regulatory affairs, quality management and design & development of medical devices and biocides, as well as cleaning validation.
MDC Buhmann
Geissfluhstrasse 8
4500 Solothurn, Switzerland
CH: +41 78 268 42 16