Thomas Regulatory
10001 New York City , NY, USA, New York CITY, 10001
1 561 898 0260
Thomas Regulatory
Owners and operators of
businesses involved in the manufacture and distribution of medical devices,
drugs, combination products, dietary supplements, or cosmetics in the United
States must register with the FDA annually. These administrative tasks, FDA
medical device consultant,
are time-consuming and often overlooked, leading to delays and errors in
registration certificates. Our Clinical Evaluation Report
Consultant is the results of your medical device
clinical evaluation process.
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