Top Industry News
- Electronic Application form (eAF) updated version 1.20
- New guidance details FDA's benefit-risk framework for device compliance, enforcement decisions
- Medical devices: European council confirms deal with EP
- FDA Issues final rule on symbols for device labels
- FDA offers new draft guidance on bioequivalence studies for 19 generics, 19 revisions
- FDA issues draft guidance on critical quality attributes for chewable tablets
- FDA - Drug establishments current registration site(updated)
- Novartis aims to nearly triple biosimilar drugs on market by 2020
- UK MHRA finds GMP deviations at two facilities