Regulatory Affairs

I provide competent and reliable support for all questions regarding the marketing authorization and lifecycle management of medicinal products in Switzerland.

Consulting on all regulatory matters
Development and implementation of individual regulatory strategies
Preparation as well as formal and content-related review of marketing authorization dossiers for Switzerland
Preparation of expert reports, statements, and regulatory reports
Complete regulatory support for products throughout their entire lifecycle
Support for variations, renewals of marketing authorizations, and other procedures