Thinking About the FDA’s Alternative Summary Reporting Program | Drug & Device Law
Bexis has been updating the preemption chapter of his treatise on drug/device product liability litigation. He came across several preemption| Drug & Device Law
Bexis has been updating the preemption chapter of his treatise on drug/device product liability litigation. He came across several preemption| Drug & Device Law
Requirements for reporting medical device problems, including malfunctions and adverse events (serious injuries or deaths) associated with medical devices.| U.S. Food and Drug Administration
