Panacea Biotec reaches settlement with Apotex
Apotex will also pay US$ 2.5 million upon receipt of final USFDA approval of the ANDA that is the subject of the Collaboration Agreement for Paclitaxel Protein-Bound Particles for Injectable Suspension
Apotex will also pay US$ 2.5 million upon receipt of final USFDA approval of the ANDA that is the subject of the Collaboration Agreement for Paclitaxel Protein-Bound Particles for Injectable Suspension
Aarti Pharmalabs becomes 6th Indian Pharma/CDMO to earn SBTi approval for all 3 Scopes since 2022 demerger
Revenue up 11% to Rs 5,768 crore as compared to Rs 5,197 crore
Designation was based on early efficacy data demonstrating an 83.3% (10/12) overall response rate and a 50% (6/12) complete response rate, with a well-managed safety profile in Relapsed/Refractory Hodgkin Lymphoma patients
HYMPAVZI’s approval is based on Phase 3 study results demonstrating non-inferiority and superiority compared to routine prophylaxis in eligible patients with hemophilia A or B without inhibitors
For Q2, Akums reported a consolidated total income of Rs. 1,046.6 crore
Lyka has received the CDSCO approval for manufacturing and marketing of Pregabalin Gel 8% w/w
The sample seized by CDSCO is not manufactured by Torrent and is in fact non-genuine and spurious
Aragen Life Sciences is the first Indian CRDMO to receive SBTi approval
At 10 years, more than one-third (34.0%) of patients with advanced melanoma were alive after treatment with KEYTRUDA, compared to 23.6% of patients treated with ipilimumab
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