As a contract research organization and consultancy dedicated to accelerating medical innovation, Beaufort, LLC, believes that sharing knowledge and expertise is critical. We provide the following resources to help propel a deeper understanding of FDA regulatory consulting, quality assurance and compliance, and clinical research.
Find external resources for FDA information including FDA quality systems regulations, medical device registration and listing instructions, premarket notification search, and the FDA CFR Title 21 database.
A number of standards organizations provide norms and guidelines for companies in the pharmaceutical, medical device, in vitro diagnostics, and biologics industries. Here, find links to many of those resources.
Find additional resources for national and international agencies and associations providing guidance in the areas of quality, statistics, clinical research, regulatory affairs and more.
Beaufort, LLC, has a proven track record of providing creative solutions and practical strategies for its clients. Here, see how Beaufort’s experts have met the clinical research, quality assurance and compliance, and regulatory affairs challenges of healthcare companies around the world.
Beaufort’s experts are actively engaged in dialog on current research topics and frequently share their insight at industry meetings. We provide some of their recent presentations as a resource for you.
We believe that by working closely with our clients and customizing every solution, we can anticipate their changing needs and stay ahead of industry trends. When we introduce a new service or one of our experts appears in the news media to provide insight on a current topic, you’ll find that information here.