Jubilant Pharmova announces completion of USFDA audit of Radiopharmaceuticals manufacturing facility at Montreal
The USFDA has issued 5 observations pursuant to the completion of audit
The USFDA has issued 5 observations pursuant to the completion of audit
Yonghe as the CDMO partner will provide production process development and cGMP manufacturing services for Ablaze
With the receipt of the EIR, the inspection stands successfully closed.
The study will run across 18 sites and enroll roughly 200 patients over 24 months
Harbour BioMed brings advanced antibody discovery platforms to the table
Dr. Brown brings extensive international experience in oncology and radiopharmaceutical development,
Jubilant's Radiopharma Business to expand positron emission tomography radiopharmacy network
Acquisition encompasses a portfolio of RLT programs across a range of solid tumor indications
To accelerate the development of next-generation radioconjugates to treat cancer
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