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Sentynl Appoints myTomorrows as Global Provider to Expand Managed Access Program

Sentynl Appoints myTomorrows as Global Provider to Expand Managed Access Program

Sentynl Therapeutics, a biopharmaceutical company based in the USA and wholly owned by Zydus Lifesciences, has appointed myTomorrows as the global provider for its Managed Access Program (MAP).

| 11/12/2025 | By 145

MMV Joins iiCON to Boost Infectious Disease Drug Research and Manufacturing Innovation

MMV Joins iiCON to Boost Infectious Disease Drug Research and Manufacturing Innovation

iiCON, led by the Liverpool School of Tropical Medicine (LSTM), is a global infectious disease R&D programme that unites industry, academic institutions, and clinical bodies to accelerate the development of treatments, diagnostics, and prevention technologies for infectious diseases. Its mission is to save and improve lives.

| 11/12/2025 | By 173

AST and Marchesini Group Partner to Expand Global Market Presence

AST and Marchesini Group Partner to Expand Global Market Presence

AST and Marchesini Group have formed a strategic partnership to strengthen their global market presence by combining technology and expertise in aseptic manufacturing. The collaboration aims to accelerate growth and enhance advanced, sterile production capabilities for customers worldwide.

| 11/12/2025 | By 213

Veritiv Unveils First Curbside-Recyclable Pallet Shipper for Biopharma Cold Chain

Veritiv Unveils First Curbside-Recyclable Pallet Shipper for Biopharma Cold Chain

Veritiv has launched PalletShield, the industry’s first curbside-recyclable pallet shipper built for biopharmaceutical cold chain needs. Engineered for the stringent demands of life sciences and healthcare logistics, the solution offers a sustainable alternative to EPS and PUR systems while streamlining pack-outs and reducing disposal costs.

| 11/12/2025 | By 396

Eli Lilly Expands USA Manufacturing with Alabama Plant

Eli Lilly Expands USA Manufacturing with Alabama Plant

The site will focus on producing synthetic and peptide-based medicines, including Lilly’s first oral GLP-1 weight-loss therapy, Orforglipron, which the company expects to submit for regulatory approval early next year.

| 11/12/2025 | By 164

Government's Price Control Measures on Pharma Products Deliver Annual Savings of INR 25,000 Crore

Government's Price Control Measures on Pharma Products Deliver Annual Savings of INR 25,000 Crore

The National Pharmaceutical Pricing Authority (NPPA) has fixed ceiling prices for 935 scheduled formulations as of early December, resulting in estimated annual savings of around INR 3,802 crore for the public.

| 11/12/2025 | By 187

Xcell Biosciences and Culture Biosciences Partner to Improve Cell Therapy Quality with AI and ML

Xcell Biosciences and Culture Biosciences Partner to Improve Cell Therapy Quality with AI and ML

Xcell Biosciences has partnered with Culture Biosciences to integrate AI- and ML-driven analytics into cell therapy development. The collaboration leverages a cloud-based platform capable of multivariate analysis, enabling real-time optimisation to enhance cell therapy performance and improve patient outcomes.

| 10/12/2025 | By 242

Novo Nordisk Completes Acquisition of Akero Therapeutics

Novo Nordisk Completes Acquisition of Akero Therapeutics

Novo Nordisk has finalised its acquisition of Akero Therapeutics, making Akero a wholly owned subsidiary. Following the transaction, Akero’s common stock will cease trading on the Nasdaq Global Select Market.

| 10/12/2025 | By 265

Japan Grants SAKIGAKE Status to AskBio's Gene Therapy Products, Boosting Global Pharma Manufacturing Momentum

Japan Grants SAKIGAKE Status to AskBio's Gene Therapy Products, Boosting Global Pharma Manufacturing Momentum

This designation underscores Japan’s commitment to accelerating breakthrough therapies that demonstrate novel mechanisms of action, strong preliminary data, and meaningful potential for addressing severe, underserved conditions.

| 10/12/2025 | By 349

FDA Qualifies First AI Tool to Accelerate Liver Disease Drug Development

FDA Qualifies First AI Tool to Accelerate Liver Disease Drug Development

The U.S. Food and Drug Administration (FDA) has qualified the world’s first artificial intelligence tool designed to speed up drug development for liver disease.

| 10/12/2025 | By 1343

 
 

 

 

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