Medical Device Industry

The “Medical Device Industry” category at AssurX focuses on the unique needs and challenges of this highly regulated sector. This section provides insights into quality management, regulatory compliance, and process optimization specifically for medical device manufacturers. Topics include navigating complex regulations, ensuring product safety, and improving operational efficiency. With AssurX’s expertise, medical device professionals can maintain compliance, enhance quality, and drive innovation, ensuring products meet stringent industry standards.

FDA Guidance on How to Address Inaccurate Online Claims Against Medical Device or Drug Manufacturers
FDA Guidance on How to Address Inaccurate Online Claims Against Medical Device or Drug Manufacturers

FDA Guidance on How to Address Inaccurate Online Claims Against Medical Device or Drug Manufacturers

AssurX Blog2014-06-24T10:11:44+00:00June 24th, 2014|

Distilling the FDA Guidance on How to Address Inaccurate Online Claims Against M [...]

FDA Acts to Harmonize Global Adverse Event Reporting
FDA Acts to Harmonize Global Adverse Event Reporting

Medical Device Industry

FDA Guidance Advises Device Makers to Think About Home-Use

FDA Spreads Regulatory Love Nationwide

Time to Take a Closer Look at FDA MDDS Moves

FDA Lets MDDS Off The Regulatory Hook

FDA Guidance on How to Address Inaccurate Online Claims Against Medical Device or Drug Manufacturers

FDA Guidance on How to Address Inaccurate Online Claims Against Medical Device or Drug Manufacturers

FDA Acts to Harmonize Global Adverse Event Reporting

FDA Acts to Harmonize Global Adverse Event Reporting

Medical Device Warning Letter Round-Up: FDA Won’t Take No For an Answer

The Six C’s of Document Management Best Practices for Life Sciences

Partnership of Productivity Tools Will Allow You to Focus More on Creating Quality Products

Medical Device Industry Endures Tough 2013; 2014 Prospects Not Much Better