Скачать с ютуб The Q-Submission Program | Proxima CRO в хорошем качестве

The Q-Submission Program | Proxima CRO

Grace Carrell, one of Proxima's Regulatory Associates, is here to share a quick overview of the FDA's Q-Submission Program! This program features useful tools that emerging MedTech companies should familiarize themselves with in order to find the most efficient path toward market approval. Looking to learn more? Check out our in-depth look at a few Q-Submission types: Pre-Submissions    • What Are Pre-Submissions? | Proxima CRO   Informational Meetings    • Breakthrough Device Designation Timel...   Breakthrough Device Designation    • Breakthrough Device Designation | Pro...   Proxima works with emerging biotech and medical device companies across all phases of development. As a contract research organization, we organize our team in two distinct areas: early-stage advisory consulting and all-inclusive clinical trial services. The service you need. The speed you want. The attention you deserve. Thanks for watching! Website: https://proximacro.com/ Twitter: @ProximaCRO LinkedIn:   / proxima-clinical-research   Business email: [email protected] Produced by: Julian Lara, Videographer & Graphic Designer Brandon Clements, Production Manager Devin Finch, Creative Director