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China's National Medical Products Administration Approves New Oncology Drug Focusing on Targeted Therapy
Sunday, August 31, 2025The National Medical Products Administration NMPA has granted approval for a novel oncology drug targeting specific molecular pathways a significant advancement in targeted cancer therapy
India Announces New Guidelines for Biosimilars Development to Accelerate Market Entry
Sunday, August 31, 2025
China's National Medical Products Administration Approves Innovative Alzheimer’s Treatment
Saturday, August 30, 2025
India's Department of Biotechnology Announces New Funding for Biopharmaceutical Research
Saturday, August 30, 2025
IQVIA and Flagship Pioneering form collaboration to support growth of life sciences companies
Friday, August 29, 2025IQVIA has announced a strategic collaboration with Flagship Pioneering The partnership aims to accelerate the growth of Flagships network of biopharma companies by using IQVIAs expertise and resources These include access to extensive data advanced a...
D3 Bio Receives FDA Breakthrough and Orphan Drug Designations for KRAS G12C Inhibitor
Friday, August 29, 2025D Bio has announced that the US Food and Drug Administration FDA has granted Breakthrough Therapy Designation to its investigational drug DS for the treatment of adults with KRAS GCmutated nonsmall cell lung cancer NSCLC
Travere Therapeutics Receives Approval for Updated REMS Labelling of FILSPARI® in IgA Nephropathy
Thursday, August 28, 2025Travere Therapeutics has announced that the US Food and Drug Administration FDA has approved updated Risk Evaluation and Mitigation Strategy REMS labelling for FILSPARI sparsentan the only dual endothelin
Pfizer and BioNTech’s COMIRNATY® COVID-19 Vaccine Receives Approval for Older Adults and High-Risk Groups
Thursday, August 28, 2025Pfizer and BioNTech have received approval from the US Food and Drug Administration FDA for their LPadapted monovalent COVID vaccine COMIRNATY LP
Sandoz Launches Rivaroxaban in Germany, Broadening Affordable Antithrombotic Access
Thursday, August 28, 2025Sandoz has introduced its generic version of rivaroxaban in Germany making available new strengths of mg mg and mg under the brand Rivaroxaban A Pharma
Heidelberg Pharma’s Partner Telix Receives FDA Complete Response Letter for TLX250-CDx
Thursday, August 28, 2025Heidelberg Pharma announced that its licensing partner Telix Pharmaceuticals has received a Complete Response Letter CRL from the US Food and Drug Administration FDA for its Biologics License Application BLA for TLXCDx