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.”
Dendrite International, Inc., a leading provider of pharmaceutical industry
solutions, today announced a comprehensive three-year agreement to provide SINE
Pharmaceutical Company Co., Ltd, a subsidiary of Shanghai Pharmaceutical Group
Co., Ltd (SPGC) and pioneer in China's growing pharmaceutical market, with components
of Dendrite's Sales Solutions.