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Over-the-Counter (OTC) drug products are heavily regulated by the U.S. FDA and must be marketed legally and appropriately. Pharmaceutical companies enlist the help of experts who provide FDA OTC drug consulting services. The FDA allows for two regulatory pathways to legally market OTC drug products; the New Drug Application (NDA)/ Abbreviated New Drug Application (ANDA) and the OTC drug monograph. Call : 08133332950 Visit : https://biotechresearchgroup.com/marketing-otc-drugs-legally/