For pharmaceutical and medical device manufacturers, computerized systems validation is vital. The following are three areas businesses must fine tune to ensure computerized labeling systems meet the stipulations of the new GxP regulations.
Incorporating bioinformatics platforms can ease the burden of tracking, analyzing and managing the use of antibiotics.
Although the cloud offers great value for medtech manufacturers and device users, it also creates new challenges.
Adopting new technology to ensure the health and safety of patients shouldn’t adversely affect security and privacy.
New health-related data is arriving almost daily. Making sense of it all is a huge challenge.
The immense challenges posed by the coronavirus pandemic are fueling interest in cloud computing among vaccine researchers, clinicians, healthcare companies and patients across Asia.
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.
Growth of the Asian cloud computing market is expected to accelerate as healthcare providers streamline their operations in today’s paperless world.
It’s more than a bolt-on. Here’s a smart approach to integrate medical devices into connected systems.