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Camargo Pharmaceutical develops and executes comprehensive drug development programs tailored to meet the needs of your specific compound. Our expert team has years of experience in the full spectrum of drug development.
Our goal is to work with your team to develop a comprehensive program including a timeline with important milestones and costs. We manage every facet of your program: formulate and test the drug product, conduct clinical studies, and guide you through the FDA application submission process-specializing in 505(b)(2). The 505(b)(2) submissions have special requirements; you need the experts at Camargo to guide you through the process.
Increase your speed-to-market with Camargo as your strategic partner.
Drug Development Services
• Pre-clinical
• Feasibility assessments
• CMC/CMO services
• Clinical program development
• Pharmacokinetics
• Phase I
• Phase II
• Phase III
• Phase IV
• Regulatory review/preparation/submission
• IND
• NDA
• ANDA
• 505(b)(2)
Therapeutic Expertise.
Camargo's associates are accomplished in a wide variety of therapeutic areas:
• Anti-fungal
• Anti-infective
• Anti-inflammatory
• Cardiovascular
• Central nervous system
• Contraception
• Dental
• Dermatology
• Diagnostics
• Endocrinology
• Female sexual dysfunction
• Gastrointestinal
• Genito-urinary
• Hormone replacements
• Immunology (including allergy)
• Infectious disease
• Migraine
• Oncology
• Pain management/anesthetics
• Respiratory
• Sleep disorders
• Women's health