By devoting our entire practice to pharmaceutical and biologics work, RMMS has become intimately familiar not only with our clients' legal issues, but also the business, legislative, regulatory, and political hurdles facing our clients.  

We provide a full range of counseling and litigation services to our clients, beginning as early as the product selection stage; continuing through the product development and submission stages, covering the agency review and approval process; encompassing all stages of patent and regulatory litigation, including settlements; and extending through the commercialization of the product.  We also assist our clients in exploring, negotiating, and closing related business agreements, such as joint development agreements, active pharmaceutical ingredient (API) and finished dosage form supply agreements, licensing agreements, and co-promotion and marketing agreements.  

Learn more about our extensive services and industry expertise in these areas: