Regulatory Services
Providing you with 505(b)(2) and ANDA regulatory strategy and filing services.
In addition to developing your product, we can manage all the necessary regulatory requirements to get your concept into the clinic and commercialized. Many of our clients are clinical stage companies who benefit from our full-service drug development package for NDA or ANDA filings.
Vici provides a range of integrated or stand-alone FDA regulatory services:
- 505(b)(2) FDA Regulatory Strategy & Consulting
- Pre-IND, IND, and NDA writing and project management
- ANDA writing and filing
- Commercial Product regulatory support
Partnering with a full-service drug development company like us allows you to focus on what you do best: innovate and commercialize. Call us today to discuss streamlined, cost-effective regulatory solutions tailored for you.
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Our industry experts at Vici Health Sciences can bring your product to market faster.
Schedule a free consultation for your project with one of our experts.