Designed as an “AI-as-a-Service” platform, VECURA aims to reduce the traditional therapeutic drug discovery timeline of 10–12 years to just a few hours.
The U.S. FDA issued a Form 483 with five observations
Earlier in July 2025, Dazublys has received the marketing authorisation in the European Union from the European Commission
The companies will now begin detailed contract negotiations and proceed with necessary consultations and approval processes
She was Group Chief Marketing Officer at CKA Birla Group in her last role
Vevzuo is authorized for the prevention of skeletal related events in adults with advanced malignancies involving bone
Over 100 million cartridges of rh-insulin supplied to Malaysian health ministry; 345,000+ patients served
The approval is based on a comprehensive package of analytical, nonclinical, and clinical data
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