Skip to Main Content
It looks like you're using Internet Explorer 11 or older. This website works best with modern browsers such as the latest versions of Chrome, Firefox, Safari, and Edge. If you continue with this browser, you may see unexpected results.

Grey Literature: Drug & Device

What is grey literature? How do I find Grey Literature?

Drug & Device Regulatory Information

Drugs & Medical Devices have registries to keep up with their progress through trial and use after they are FDA approved. 

Drug & Device Regulatory Information Resources:

OpenTrialsFDA (Beta)

OpenTrialsFDA works on making clinical trial data from the FDA (the US Food and Drug Administration) more easily accessible and searchable. 

OpenTrialsFDA extracts the relevant data from the FDA documents, link it to other clinical trial data and present it through this new user-friendly web interface.

US Food and Drug Administration (FDA)

The Food and Drug Administration is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of our nation's food supply, cosmetics, and products that emit radiation.

Drug Regulations can be found here & Medical Device Regulations can be found here.