She gradually increased her dosage, eventually up to 10 pills a day, resulting in addiction, Chang said. Food and Drug Administration Deputy Director-General Wang Der-yuan center, speaks at a news ...

CBL-514 is the first and only drug to receive EMA Orphan Drug Designation for Dercum's disease treatment. - CBL-514 received both FDA Orphan Drug Designation and Fast Track designation for Dercum's ...

Emulsifiers are additives that help oil and water mix, making smoother food products. But they may carry a big downside for ...

Subsidies of up to NT$100,000 are also available for chain stores to reimburse the cost of printing new labels and materials, it said. Businesses for which at least five stores display proper labeling ...

Cardiol has received Investigational New Drug Application authorization from the U.S. Food and Drug Administration (FDA) to conduct clinical studies to evaluate the efficacy and safety of CardiolRx in ...

Santen Pharmaceutical and Arctic Vision have signed a commercial collaboration agreement for the ARVN001to treat uveitic ...

SAN DIEGO, CA / ACCESSWIRE / November 6, 2024 / Ainos, Inc. (NASDAQ:AIMD)(NASDAQ:AIMDW) ('Ainos', or the 'Company'), an innovative healthcare company focused on advanced AI-driven point-of-care ...

Donald Trump won in large part because of voters' frustration with the economy. But when he enters office, he will inherit an ...

The report said an approval from Taiwan's Food and Drug Administration (TFDA) for the study is expected in next quarter, with the trial set to start around April 2025 and completion in December 2026.