FDA Attorney Services - How to Choose an FDA Attorney

Individuals around the world are looking for the best nutritional content in the packed food and supplements that they want to consume. Everybody is cautious of their weight while some individuals are allergic to specific food components. Even so, there are standards set by the FDA to ensure all food and drug products meet the required minimum values. Hence, either way; as a producer or consumer, you may have to make or respond to FDA Nutrient Content Claims to demand that you get a relevant attorney to help you win.

Whether you are looking for an FDA attorney, FDA lawyer, or FDA consultant, we can help! Call us at (305) 507-9843. You can also visit our website for more details about our FDA attorney services.

FDA Attorney Services - Premarket Approval Services

The FDA regulates medical devices on a three-tier, risk-based approach. Class III medical devices, or high-risk medical devices, are typically subject to the most stringent regulatory requirements, including the submission of a premarket approval application (“PMA”). Contrasted with the premarket notification process, the PMA (premarket approval) process is more rigorous because it requires a device sponsor to demonstrate that its device is safe and effective for its intended use, based on scientific evidence.

 Do you have any questions about your device or an FDA regulatory attorney can help you with the premarket approval process? Please contact us today at (305) 507-9843 for the best FDA attorney services. You can also visit us online for more details.

FDA Lawyer Services - How to Get FDA Approval

To get FDA approval, drug manufacturers must conduct lab, animal, and human clinical testing and submit their data to the FDA. FDA will then review the data and may approve the drug if the agency determines that the benefits of the drug outweigh the risks for the intended use.

For additional questions regarding how to get FDA approval and other FDA regulations, please feel free to contact Shehadeh Giannamore, PLLC at (305) 507-9843. You can also visit our website for more details about our FDA lawyer services.

FDA Consultant Services - Outer Packaging Requirements and FDA Regulatory Assistance

The FDA has particular requirements for the labels of the products it regulates. In particular, the FDA requires certain statements to be made on the Principal Display Panel (PDP) of many FDA-regulated products, such as the Net Quantity of Contents, Statement of Identity, etc. However, it must be noted that the label requirements differ based on product classification. When products are packaged in both outer and inner containers, the general labeling requirements may vary.

If you would like to know more about outer packaging requirements or how we can help you ensure that your labels comply with FDA regulations, please feel free to contact us at (305) 507-9843 for the best FDA consultant services. You can also visit us online for more details.