We provide comprehensive services to guide you through the development and execution of a program strategy, across all stages of development and life cycle management, for drugs, biologics, and medical devices.
Through decades of focused therapeutic expertise, strong site and investigator relationships and an insider’s understanding of the regulatory landscape, Rho’s team of experts ensure consistent trials—traditional, virtual, and hybrid—that run smarter and more efficiently.
Marketing application submissions, including NDAs, BLAs, and MAAs, are the culmination of years of research and the final hurdle before a product makes it to market. Let our integrated team of experts get your product across the finish line.
- Regulatory Agency Meetings
- Integrated Analysis Development
- Marketing Application Development
- Submissions & Publishing
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