The FDAnews report EU MDR Compliance can help. Our editors have combed through the regulations, picking out the most minute compliance points and building them into a checklist of 200+ requirements you can use to confirm that you are satisfying all the EU mandates for device manufacturing.
The FDA said it “continues to receive a high volume of pre-submissions from industry requesting feedback about the necessary data to support pivotal clinical studies and marketing applications for a wide variety of device designs intended for weight loss.”
Kurve Technology, Inc., a leader in nasal drug delivery devices, today announced
the signing of an agreement with development-stage pharmaceutical company DARA
BioSciences, Inc. (DBI). DBI focuses on the treatment of metabolic diseases,
central nervous system disorders and medical devices.