On July 8, the U.S. Food and Drug Administration (“FDA”) announced its updated guidance, “Addressing Misinformation About Medical Devices and Prescription Drugs: Questions and Answers,” which provides recommendations and examples for firms who choose to address misinformation about or related to their approved or cleared drug or device……
By: Sheppard Mullin Richter & Hampton LLP
By: Sheppard Mullin Richter & Hampton LLP