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Latest Industry News - Page 338

USFDA Approves Bionpharmas Generic HIV Drug Etravirine

Merck gets USFDA nod for WINREVAIR (sotatercept-csrk) for adults with pulmonary arterial hypertension

Ruchika Sharma27 March 2024 11:51 AM IST
Rahway: Merck, known as MSD outside of the United States and Canada, has announced that the U.S. Food and Drug Administration (FDA) has approved...
CDSCO Panel Approves IQVIAs Protocol Amendment Proposal For Anti-cancer Drug Xevinapant

CDSCO Panel Approves IQVIA's Protocol Amendment Proposal For Anti-cancer Drug Xevinapant

Dr. Divya Colin27 March 2024 5:30 AM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has approved the drug major...
Indoco Remedies arm begins commercial production of Pharmaceutical Intermediates

Indoco Remedies arm begins commercial production of Pharmaceutical Intermediates

Ruchika Sharma26 March 2024 3:30 PM IST
Mumbai: Warren Remedies Private Limited, a Wholly Owned Subsidiary of Indoco Remedies Limited has commenced its commercial production from its...
AstraZeneca Gets SEC Nod to Update Lokelma Prescribing Information for Hyperkalemia Treatment

AstraZeneca Pharma India names Vinay Sharma as Business Unit Head

Ruchika Sharma26 March 2024 2:12 PM IST
Bangalore: AstraZeneca Pharma India Limited has announced the appointment of Vinay Sharma as Business Unit Head - Rare Disease unit with effect...
AstraZeneca Saphnelo subcutaneous self-administration recommended for approval in EU by CHMP for systemic lupus erythematosus

AstraZeneca Ultomiris gets USFDA approval for adults with neuromyelitis optica spectrum disorder

Ruchika Sharma26 March 2024 12:52 PM IST
Ultomiris, a long-acting C5 complement inhibitor, provides immediate, complete and sustained complement inhibition.
Health Ministry Reduces Clinical Trial Approval Time from 90 to 45 Days

Bharat Biotech begins clinical trial of Tuberculosis vaccine MTBVAC in India

Ruchika Sharma26 March 2024 12:34 PM IST
Hyderabad: Clinical trials of MTBVAC, the Spanish tuberculosis vaccine, the first live attenuated vaccine of Mycobacterium tuberculosis isolated...
AstraZeneca Saphnelo subcutaneous self-administration recommended for approval in EU by CHMP for systemic lupus erythematosus

CDSCO Panel Approves AstraZeneca's Protocol Amendment Proposal For Anti-cancer Drug Osimertinib

Dr. Divya Colin25 March 2024 5:00 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has approved the drug major...
Lupin Manufacturing Solutions, PolyPeptide Group forge long term Peptide alliance

Bayer, Thermo Fisher Scientific join hands to increase patient access to precision cancer medicines

Ruchika Sharma25 March 2024 12:30 PM IST
Berlin: Bayer AG and Thermo Fisher Scientific Inc. have announced a collaboration to develop next-generation sequencing (NGS)-based companion...
Aurobindo Pharma arm to acquire 20% additional ownership in Luoxin Aurovitas for Rs 45 crore

Lonza to buy large-scale biologics Vacaville site from Roche for USD 1.2 billion

Ruchika Sharma25 March 2024 10:00 AM IST
Basel: Lonza, a global manufacturing partner to the pharmaceutical, biotech and nutraceutical markets, has announced it has signed an agreement...
Pfizer Slapped With Rs 8.79 Cr GST Demand Over Alleged ITC Irregularities, Plans Appeal

Pfizer Gets CDSCO Panel Nod To study anti-cancer drug Lorlatinib

Dr. Divya Colin24 March 2024 5:45 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has approved the drug major...
Zydus

Zydus Lifesciences receives tentative approval from USFDA for Letermovir Tablets

Ruchika Sharma24 March 2024 2:30 PM IST
Letermovir tablets are used to prevent disease caused by a virus called cytomegalovirus in people who have received a bone marrow transplant or kidney...
Novartis concludes acquisition of Tourmaline Bio

Novartis Fabhalta gets positive CHMP opinion as first oral monotherapy for adult patients with paroxysmal nocturnal hemoglobinuria

Ruchika Sharma24 March 2024 2:30 PM IST
Basel: Novartis has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a...
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Editorial

SURPASS-2- Tirzepatide vs Semaglutide in Type 2 Diabetes

SURPASS-2- Tirzepatide vs Semaglutide in Type 2 Diabetes

Obesity-Prediabetes Duo: Why Clinicians Must Intervene Early?

Obesity-Prediabetes Duo: Why Clinicians Must Intervene Early?

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

Regulatory Approval Granted for Reformulated Ranitidine

Regulatory Approval Granted for Reformulated Ranitidine

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Medical Bulletin 6/February/2026

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