6、Off work due to illness.（因病请假、以病休息）7、Approved absence for medical reasons.（经批准的带薪病假）8、Sick day.（病假日，即离职期间病假的天数）9、Return-to-work clearance.（返岗审查程式）三、其他表达 time away from work because of illness.病假英文例句：1、This term is...
Returning to work after medical leave is a challenge. Here's how to make your transition from medical leave to work much smoother.
Medical Return Trip Improvement Program Medical Returnee medical revalidation medical revalidation Medical Revenue Management Association of America Medical Review Board Medical Review Institute of America Medical Review Officer Medical Review Officer Medical Review Officer Certification Council ...
Using the AlphaSense platform, we uncover and analyze the top medical device trends around the world. Here’s what to expect in the medical device space in 2024.
Jeff Young
One hundred patients with second degree bleeding piles were randomized prospectively to either rubber band ligation (n = 54) or infrared coagulation (n = 46). Parameters measured included post-operative discomfort and pain, time to return to work, relief in incidence of bleeding, and recurrence ...
To facilitate a move to a new location, XHTCM built a brand-new data center and disaster recovery site from the ground up with Lenovo ThinkSystem servers, powered by Intel® Xeon® Scalable processors. Since the move, the hospital has achieved always
Olympus’ new EVIS X1 endoscopy system and two compatible gastrointestinal endoscopes- the GIF-1100 gastrointestinal videoscope and the CF-HQ1100DL/I colonovideoscope, got FDA clearance in 2023. The CF-HQ1100DL/I colonovideoscope is used for the lower digestive tract, including the anus, rectum,...
Everly Health’s Cindy R. Kent has marked her first months as Chief Operating Officer by helping lead the company through incredible growth: in fact, Everly Health recently announced it has enabled more than 45 million COVID-19 tests since the onset of the pandemic in addition to countless ad...
Successful completion of design verification marks the time when the entrepreneur can complete and submit a regulatory submission as required by the path to market clearance. In the US, this submission may be a FDA 510(k) application or an FDA investigational device exemption submission. Outside ...