All medical devices sold in the United States are regulated by the U.S. Food and Drug Administration (FDA). More specifically, any medical device manufactured, repackaged, relabeled, and/or imported by any company or firm to sell in the U.S. has to meet FDA regulations.
News & Events
As a medical contract manufacturing company, the BMP Medical Team will be attending the MD&M West Expo at the Anaheim Convention Center in California this February. As North America’s largest annual MedTech event, MD&M West connects thousands of advanced design and manufacturing professionals, engineers, executives, and suppliers. It offers an opportunity to learn from industry… Read more »
As a medical contract manufacturer, the BMP Medical Team is excited to attend the BIOMEDevice Expo at the Boston Convention & Exhibition Center in Massachusetts this April. As New England’s largest annual MedTech event, BIOMEDevice connects thousands of medical device design and manufacturing professionals, engineers, executives, and suppliers. It offers an opportunity to learn from… Read more »
As an OEM medical device manufacturer, the BMP Medical Team will attend the DeviceTalks Exhibit at the Westin Waterfront in Boston this October. This event is a can’t-miss opportunity for companies in the MedTech community as it fosters the exchange of ideas, insight as well as technology information among biomedical industry pioneers.
Medical manufacturing companies know the consequences of failing to adhere to FDA (The U.S. Food and Drug Administration) regulations can have severe repercussions. One glance at the U.S. Department of Justice and the U.S. Department of Health and Human Services joint annual report on health care fraud and abuse control shows approximately $3.3 billion in… Read more »