Thailand
Intelligence de marché des dispositifs médicaux pour Thailand. Changements réglementaires, concurrents et tendances d'achats.
Signaux récents
The study evaluates the effectiveness of the BreatheMAX breathing device on secretion clearance.
MARCO OPTICAL (THAILAND) COMPANY LIMITED is registered with FDA under product code HOY.
ASAHI INTECC CO., LTD. has registered a medical device with the FDA under product code DQX.
Panasonic Manufacturing (Thailand) Co., Ltd. has FDA registration 9710575 for product code EFS.
A trial is assessing optimal dose and frequency for home photodynamic therapy using a novel LED device for onychomycosis.
A clinical trial is recruiting to test the DidgeriTU device's efficacy in reducing apnea events in non-severe OSA.
A study compares the efficacy and cost of parenchymal stapling devices versus hand sewing in lung lobectomy.
Thai police arrested a 33-year-old Indonesian for $10 million cyber fraud after an FBI tip-off.
The article discusses how the Iran war challenges the influence of Asian middle powers, including Thailand.
Singapore leads in cyber defenses but ranks low in executive leadership on the issue.
Forest fires in Thailand and the Mekong region are causing a public health crisis due to dangerous smoke.
The Iran energy crisis is accelerating Southeast Asia's shift to electric vehicles amid rising fuel prices.
Thai hotels are customizing experiences to attract Asian travelers as European visitors decline due to the Iran war.
Well Link Bank partners with FWD Insurance for bancassurance in Macau.
WHO reports rising antibiotic resistance in gonorrhoea, urging enhanced surveillance and treatment access.
WHO's first Global Forum unites over 800 Collaborating Centres to enhance scientific collaboration for public health.
AI is revolutionizing TB screening with handheld X-ray devices in over 22 countries.
Sanitation investments drive economic growth, reduce healthcare costs, and improve productivity and tourism.
Philips recalls ALLURA Xper FD20 OR Table due to intermittent X-ray imaging issues with the foot switch.
Burlington Medical recalls Class II protective sleeves due to potential lifespan degradation.