Q3 2025 Management View CEO A. Kazimi announced a new strategic agreement: "We've entered into arrangements with RedHill ...
A new antimicrobial generic drug was approved by officials with the FDA for the treatment of canine skin infections: ...
The U.S. Food and Drug Administration (FDA) has approved two new biosimilars as reference products for Prolia (denosumab) and XGEVA® (denosumab): Stoboclo (denosumab-bmwo) and Osenvelt (denosumab-bmwo ...
The Food and Drug Administration (FDA) is launching an effort to streamline the approval process for cheaper alternative ...
6don MSN
FDA to streamline approvals for generic biological drugs in latest move targeting health costs
The US Food and Drug Administration will take steps to streamline the process to develop generic versions of complex ...
The FDA has announced new rules for the approval of biosimilar drug products that could reduce 5- to 8-year timelines by half.
Investor Frenzy Pushes Subscription Over 2x Despite Valuation Concerns Retail Investors Fuel Early Buzz as Groww IPO Sees 57% Subscription on Day 1 Democrats Push Back on GOP Claims That Biden ...
FDA approval describes when the Food and Drug Administration (FDA) deems a medical product safe and effective for its intended use based on scientific data and testing. Before people use a medical ...
The FDA just recommended tighter restrictions and the potential drug classification of kratom products containing a specific extract called 7-OH. Currently, these unregulated, non-FDA-approved ...
Alvotech, for its part, has run into repeated issues with the FDA at its Icelandic drug plant. Since the company’s biosimilar accord with Teva began, problems at the Reykjavik facility have led to two ...
The Food and Drug Administration (FDA) has put four companies on notice for marketing “unapproved fluoride-containing ingestible drugs” for use by children under the age of 3 or children at low or ...
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