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Latest Industry News - Page 336

Sudhir Mehta steps down as Director of Torrent Pharma

Sudhir Mehta steps down as Director of Torrent Pharma

Ruchika Sharma3 April 2024 4:09 PM IST
Ahmedabad: Torrent Pharma has announced that Sudhir Mehta has stepped down as Director of the Company effective 31-Mar-24. He will continue to be...
Alkem Foundation, IIT Bombay collaborate to set up advanced research centre for immunotherapeutics, regenerative medicines

Bharat Biotech, SII arm Bilthoven Biologicals collaborate to produce, supply Oral polio vaccine

Ruchika Sharma3 April 2024 1:30 PM IST
Through this collaboration, BBIL and BBio will jointly obtain the regulatory approvals and licenses required to commercially manufacture OPVs in India...
Kenvue India, API join hands to release Recommendations on Oral Fluid Electrolytes, Energy Management for Hospitalized Patients with Non-Diarrheal Illnesses

Kenvue India, API join hands to release Recommendations on Oral Fluid Electrolytes, Energy Management for Hospitalized Patients with Non-Diarrheal Illnesses

Kajal Rajput3 April 2024 1:00 PM IST
New Delhi: Kenvue, the world's largest pure-play consumer health company by revenue, released a whitepaper addressing challenges in Oral Fluid,...
AstraZeneca Saphnelo subcutaneous self-administration recommended for approval in EU by CHMP for systemic lupus erythematosus

AstraZeneca, Daiichi Sankyo Datopotamab deruxtecan application accepted in US for pretreated metastatic HR-positive, HER2-negative breast cancer

Ruchika Sharma3 April 2024 12:30 PM IST
AstraZeneca and Daiichi Sankyo's Biologics License Application (BLA) for datopotamab deruxtecan (Dato-DXd) has been accepted in the US for the...
Abbott India Hit With Rs 2.40 Cr GST Penalty Over Alleged ITC Disallowance, Plans Appeal

Abbott gets USFDA approval for TriClip TEER System for Tricuspid Regurgitation

Ruchika Sharma3 April 2024 11:46 AM IST
Abbott Park, III.: Abbott has announced that the U.S. Food and Drug Administration (FDA) has approved the company's first-of-its-kind TriClip...
Abbott India Hit With Rs 2.40 Cr GST Penalty Over Alleged ITC Disallowance, Plans Appeal

Abbott gets USFDA clearance for whole blood rapid test to help with assessment of concussion at patient bedside

Ruchika Sharma2 April 2024 5:30 PM IST
With this clearance, the i-STAT TBI test can be used to help evaluate patients up to 24 hours after injury, an advancement since those injured often...
Alembic Pharma gets tentative USFDA nod for breast cancer drug Ribociclib in March Quarter

Alembic Pharma gets tentative USFDA nod for breast cancer drug Ribociclib in March Quarter

Ruchika Sharma2 April 2024 3:17 PM IST
Vadodara: Alembic Pharma has informed in a BSE filing that the Company has received tentative approval for Ribociclib Tablets, 200 mg,...
Zydus

Zydus Lifesciences gets WHO INN approval for 'Usnoflast' as recommended name for ZYIL1

Ruchika Sharma2 April 2024 1:30 PM IST
Usnoflast (ZYIL1) is a novel oral small molecule NLRP3 inhibitor discovered at Zydus.
Lupin bags tentative USFDA nod for Migalastat Capsules

Lupin bags tentative USFDA nod for Migalastat Capsules

Ruchika Sharma2 April 2024 12:30 PM IST
Migalastat Capsules are indicated for the treatment of adults with a confirmed diagnosis of Fabry disease and an amenable galactosidase alpha gene...
Alembic Pharma ropes in Manish Kejriwal as Independent Director

Alembic Pharma ropes in Manish Kejriwal as Independent Director

Ruchika Sharma2 April 2024 11:33 AM IST
Mumbai: Alembic Pharmaceuticals Limited has appointed Manish Kejriwal as an Independent Director of the company for the period of five...
Janssen-Cilag Guselkumab receives UK nod for Crohns disease, ulcerative colitis

European Commission approves Merck Keytruda plus Chemotherapy for lung cancer

Ruchika Sharma1 April 2024 5:30 PM IST
Rahway: Merck, known as MSD outside of the United States and Canada, has announced that the European Commission (EC) has approved KEYTRUDA,...
AstraZeneca Gets SEC Nod to Update Lokelma Prescribing Information for Hyperkalemia Treatment

USFDA nod to Voydeya as add on therapy to ravulizumab or eculizumab for extravascular haemolysis in adults with rare disease PNH: AstraZeneca

Ruchika Sharma1 April 2024 3:18 PM IST
Cambridge: AstraZeneca has announced that Voydeya (danicopan) has been approved in the US as add-on therapy to ravulizumab or eculizumab for the...
PrevNext

Editorial

ROBUST Study Released: One of the Largest Beta-Blocker KAP Study Captures Place of Beta Blockers in Indian Real-World Practice

ROBUST Study Released: One of the Largest Beta-Blocker KAP Study Captures Place of Beta Blockers in...

Obesity-Prediabetes Duo: Why Clinicians Must Intervene Early?

Obesity-Prediabetes Duo: Why Clinicians Must Intervene Early?

SURPASS-2- Tirzepatide vs Semaglutide in Type 2 Diabetes

SURPASS-2- Tirzepatide vs Semaglutide in Type 2 Diabetes

Efficacy and Safety of Dapagliflozin-Vildagliptin in Indian T2DM Patients with CV Risk Factors

Efficacy and Safety of Dapagliflozin-Vildagliptin in Indian T2DM Patients with CV Risk Factors

SURPASS-2: Superior HbA1c and Weight Reduction With Tirzepatide vs. Semaglutide

SURPASS-2: Superior HbA1c and Weight Reduction With Tirzepatide vs. Semaglutide

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Journal Club Today

MRI Study Maps Brain Growth Across the Perinatal Period

MRI Study Maps Brain Growth Across the Perinatal Period

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Health News Today

Health Bulletin 07/February/2026

Health Bulletin 07/February/2026

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