Cencora + PharmaLex
From clinical development to marketing authorization to post-launch activities, we deliver the whole spectrum from higher value, project-based consulting, to longer, larger and holistic outsourcing solutions. We can facilitate your interactions with health authorities, find innovative pathways as well as monitor your on-going drug safety.
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With offices in more than 25 countries, comprised of scientific, regulatory and safety and compliance (GxP) experts that provide strategic guidance and regulatory support across the development and commercialization process, we streamline your time-to-market and can help reduce your time-to-revenue.