The 505(b)(2) submissions have special requirements; you need the experts at Camargo to guide you through the process. The Camargo team has years of experience in the full spectrum of drug development — not to mention a thorough understanding of the FDA and its evolving standards.
Beyond loyalty and an intense desire to please, Camargo's expertise in drug approval will put your product on the fast-track to market. Specializing in the 505(b)(2) pathway globally, our team executes a spectrum of small and large molecule development programs. We provide expert advice grounded in years of industry and regulatory experience to take you from discovery to post-approval marketing, with a full range of services for pharmaceutical and biotech development teams.
- Cost-effective solutions
- Increase speed-to-market
- Maintain regulatory compliance