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.
An analysis of 164 phase III breast cancer trials shows bias in reporting the primary endpoint and toxicity results. Thirty-three percent of the trials published between 1995 and 2011 exhibited biased reporting of the prespecified primary endpoint. Sixty-seven percent showed bias in reporting toxicity rates. Cancer Network