The Medical Device Single Audit Program (MDSAP) is a new initiative that could help you satisfy multiple regulatory requirements with a single audit. Read on to see if this program is right for your business and what you need to do to prepare. One Audit to Accommodate...
The deadline to comply with the new Medical Devices Regulation (MDR) is fast approaching. If you sell medical devices in the European Union, it’s time to develop a successful transition strategy. MDD vs. MDR: What’s Changing From the introduction of software medical...
