The US Food and Drug Administration plans by 3 April to suspend all domestic good manufacturing practice surveillance and non-critical for-cause and pre-approval inspections for the duration of the novel coronavirus public health crisis as part of decision to require all eligible employees to work remotely
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on HBW Insight for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?