Demand for medical devices and health care products for prevention, diagnosis, and treatment, particularly of those that prevent or mitigate the risk of infection has reached an unprecedented level during the COVID-19 pandemic. We are currently experiencing unprecedented levels of interest in consulting services related to COVID-19 Emergency Use Authorizations (EUA) for products like PPEs, hand sanitizer & surface disinfectants, medical device establishment registration and listing, and authorizations for over-the-counter drugs, dietary supplements, and natural health products. It is our duty as a regulatory consultant to medical product industry partners to get these vital and life saving products delivered to the market for u seat the earliest.
As we navigate the complex situation involving COVID-19 pandemic, our company is committed and has taken all necessary measures to ensure the health and safety of our team members and our clients. Our company remains fully operational and has invested in the necessary technological infrastructure for our workforce to be able to work remotely and respond to the needs of our industry partners immediately. We strive to provide exceptional service and serve the needs of our customers to the best of our ability. As your FDA Consultant, it is our duty to do what we can to help you get these vital products to the market at the earliest. If you require a regulatory or scientific consultation or have a product that requires registration or interested in importing a COVID-19 related product from overseas for the US market, please get in touch with us immediately. We will be able to help you.
In order to ensure that we provide consistent and quality service to each of our client and get in touch with you at the shortest possible timeframe, we request you to complete the following form and submit it. As soon as we receive your consultation request, one of our FDA 510(k) consultants will get in touch with you quickly.
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