At Mejia Shehadeh Giannamore, PLLC, we assist our globally-based clientele with a wide range of regulatory issues, including premarket notifications, or 510(k) submissions, removals from import alerts, reconditioning requests, responses to warning letters and a number of other services. More information about the types of services we provide may be accessed by clicking on the links on the sidebar to the right.
In order to help our clients establish compliance with federal laws and regulations at the outset, we also provide reviews of products and marketing materials to ensure that these products are compliant with federal laws before they are marketed and sold in the United States. These reviews include ingredient and label reviews for many different types of products in all FDA-regulated industries. Some of the FDA-regulated products that we provide assistance with are foods, dietary supplements, medical devices, cosmetics and over-the-counter (OTC) drugs.
Establishing and maintaining FDA compliance with respect to the following:
- Dietary Supplements
- Medical Devices
- Over-the-Counter (OTC) Drugs
For more information about our services or how a FDA regulatory attorney may help you, please contact us.