Inpharmatis offer service "Regulatory Affairs"

Inpharmatis delivers full-spectrum regulatory affairs services—including drug development and vigilance—to pharmaceutical, medical device, food supplement, cosmetic, and biotech clients, with core expertise in Europe and the CIS extended to the US, Latin America, and select other regions through partner networks. A multidisciplinary consultant team supports marketing authorization applications for active substances and human medicines across the full product life cycle, covering submission strategy advice, life-cycle regulatory planning, and preparation, review, filing, and management of submissions.