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Researchers are working on a digital pill to manage opioid usage among patients. They are equipped with sensors that alert doctors whenever patients pop a... [Read More]
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The Food and Drug Administration (FDA) recently approved the first digital pill that tracks if patients have taken their medication. Our experts weighed in on the potential... [Read More]
* U.S. Food and Drug Administration (FDA) grants Alnylam breakthrough therapy designation (BTD) for Patisiran for the treatment of hereditary ATTR (HATTR) amyloidosis with polyneuropathy... [Read More]
LAST WEEK IN REVIEW: Monday, Nov. 13th – Friday, Nov. 17th It was a busy week at the Food and Drug Administration (FDA), with Commissioner Dr. Scott... [Read More]
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Add prescription pills to the growing list of IoT devices. The US Food and Drug Administration (FDA) has approved a "digital" prescription pill with an... [Read More]
HEMLIBRA® di Chugai ottiene la prima autorizzazione rilasciata a livello mondiale da parte dell'ente statunitense preposto al controllo dei farmac... [Read More]
Chugai Pharmaceutical Co., Ltd. (TOKYO:4519) announced today that the U.S. Food and Drug Administration (FDA) has approved the bispecific antibody emi... [Read More]
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The U.S. Food and Drug Administration (FDA) has officially granted its approval for a newfangled tracking device that pharmaceutical companies can now legally manufacture into... [Read More]
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an herb that some people use to treat pain, stress, anxiety, and even opioid withdrawal. Citing 36 deaths associated with products containing Kratom, the FDA... [Read More]
* Arbutus' LNP licensee Alnylam initiates rolling submission of New Drug Application (NDA) to U.S. Food and drug Administration (fda) for Patisiran... [Read More]
Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), announced today that the U.S. Food and Drug Administration (FDA) has approved HEM... [Read More]
Company Plans to Complete Submission by Year-End... [Read More]
* Alnylam initiates rolling submission of new drug application (NDA) to U.S. Food and drug administration (FDA) for patisiran for the treatment of hereditary ATTR... [Read More]
coined "birth control pills" or "the Pill" —were approved by the Food and Drug Administration (FDA) and hit the market.¹  ... [Read More]
Not following medicine as prescribed can be costly — like $100 billion to $289 billion, as reported by The Atlantic in 2012. Not only that,... [Read More]
The U.S. Food and Drug Administration (FDA) today announced its approval of an electric stimulation device that will help reduce the withdrawal symptoms of opioid... [Read More]
Welcome to Digital Health Briefing, a new morning email providing the latest news, data, and insight on how digital technology is disrupting the healthcare ecosystem,... [Read More]
The US Food and Drug Administration (FDA) has approved the first ever digital pill. It's high tech, and very cool, but people have big concerns. [Read More]
This week the Federal Drug Administration (FDA) approved the first "digital pill". It would allow doctors to track when patients are taking their medication. [Read More]
The Food and Drug Administration (FDA) issued a public advisory Tuesday about the herbal supplement kratom. The FDA said the supplement, marketed as an alternative... [Read More]
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