Communication and Representation: 
Landrich Group can serve as a point of contact between your company and the FDA. We can effectively communicate with the FDA on your behalf, including submitting applications, responding to queries, scheduling foreign establishment inspections, and addressing any regulatory issues that may arise. This can save you time and effort, as well as ensure clear and consistent communication with the FDA.

Local Presence:

If your company is located outside the United States, having Landrich Group as a US agent establishes a local presence in the country. This can be particularly advantageous when dealing with regulatory matters, as the US agent can represent your interests and facilitate communications with the FDA without the need for international travel or remote communication.

Regulatory Compliance:

Landrich Group as a U.S. agent, can help ensure that your device and its documentation comply with the FDA's regulations and requirements. They can review your submissions, labeling, and other relevant materials to identify any potential compliance issues, helping you address them proactively and avoid unnecessary delays or disapprovals.

Faster Response Time:

The FDA may require additional information or clarification during clearance. With Landrich Group as a U.S. agent who is knowledgeable about FDA regulations and policies, you can expect a quicker response time in addressing any requests or concerns raised by the FDA, which would help to keep the process moving forward efficiently and without undue delays.