The agency has realigned information technology, data management and cybersecurity functions, and established a new office reporting directly to the FDA commissioner.
The latest regulations for human and veterinary medicinal products, as well as medical devices, include the mandate to set up databases with detailed information about available products. These databases must be realized and implemented in the near future, and require a concerted effort now if tangible real-world benefits are to follow.
Upgrading your enterprise labeling system could play a key role in ensuring compliance.
The data that medical devices use is one of the most sensitive types of information.