In the News (2) The FDA Group's Larry Stevens to Baltimore Sun: The Regulatory Path to Warning Labels for Acid Reflux Drugs In the News (2) Inadequate CAPA Tops List of Compliance Problems for Medical Device Companies in 2016 In the News (2) 3 Important Changes in FDA's Final Guidance for Postmarket Medical Device Cybersecurity In the News (2) How the 21st Century Cures Act Will Accelerate Medical Device Approvals In the News (2) Medical Device Cybersecurity: New FDA Recommendations for Manufacturers In the News (2) Longer Orphan Drug Review Times: Advice for Manufacturers In the News (2) Press Release: The FDA Group Hires Industry Expert Brie Stoianoff as Director of Quality & Service Assurance In the News (2) CEO One on One with The FDA Group President, Nick Capman In the News (2) 8 Key Points from The FDA’s Draft Guidance on Data Integrity and CGMP Compliance