The adoption of this manufacturing process in healthcare saw a tremendous uptick in 2020.
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.
The wireless network serves as the backbone supporting patient care in every department of a healthcare facility. It is crucial to optimize and future-proof WiFi networks.
Incorporating bioinformatics platforms can ease the burden of tracking, analyzing and managing the use of antibiotics.
Top reasons for recalls include software, quality and parts issues.
The technology behind remote cardiac device monitoring is becoming more convenient, responsive and connected across the digital ecosystem—including a new smartphone app.
Medical device security needs to address the cyber-physical threats, not just patient health information risk.
Jennifer Fried, CEO of ExplORer Surgical, explains the stress that COVID-19 has placed on healthcare and the shift in how medical device reps are connecting with hospitals and healthcare providers.
Medical device recalls were up more than 31% during Q2 2020, activity that suggests recalls will reach 1200 by the end of the year, according to Stericycle’s latest recall report.
New health-related data is arriving almost daily. Making sense of it all is a huge challenge.