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Latest Industry News - Page 174

AstraZeneca Saphnelo subcutaneous self-administration recommended for approval in EU by CHMP for systemic lupus erythematosus

AstraZeneca Gets CDSCO Panel Nod To study Tezepelumab

Dr. Divya Colin13 April 2025 5:30 PM IST
New Delhi: Pharmaceutical major AstraZeneca Pharma India has got approval from the Subject Expert Committee (SEC) functional under the Central Drug...
Wockhardt

US tariffs on pharma sector would be counterproductive for Americans, says Wockhardt Chairman

Ruchika Sharma13 April 2025 3:15 PM IST
Wockhardt Chairman Habib Khorakiwala said that U.S. tariffs on pharmaceutical products would ultimately be counterproductive for Americans.The U.S....
Novartis concludes acquisition of Tourmaline Bio

Novartis plans to invest USD 23 billion over next 5 years in US based infrastructure

Ruchika Sharma13 April 2025 12:30 PM IST
East Hanover: Novartis, a global medicines company, has announced a planned USD 23 billion investment over 5 years in US-based infrastructure,...
CDSCO Panel Approves Phase IV Protocol Amendment for Bristol-Myers Squibbs Mavacamten Study

Pomalyst monopoly case: Bristol Myers wins dismissal of lawsuit

Ruchika Sharma13 April 2025 11:00 AM IST
A federal judge in New York has dismissed a proposed class action against pharmaceutical giant Bristol Myers Squibb, which accused the company of...
Morepen Labs plans to employ over 1000 professionals

Morepen Labs plans to employ over 1000 professionals

Ruchika Sharma12 April 2025 1:52 PM IST
Gurugram: Morepen Laboratories Ltd. has announced the addition of more than 1,000 professionals to its salesforce over the next three years,...
Raid at quack clinic in Telangana, drugs including Amoxycillin seized

Raid at quack clinic in Telangana, drugs including Amoxycillin seized

Ruchika Sharma12 April 2025 12:33 PM IST
Telangana: Drugs Control Administration, Telangana raided a quack's clinic in Medaram Village, Tadvai Mandal, Mulugu District and seized drugs...
Zydus Completes Agenus Deal, Launches US-Based Biologics CDMO Arm Zylidac Bio

Zydus Lifesciences bags USFDA nod for Duchenne muscular dystrophy drug Jaythari

Ruchika Sharma12 April 2025 11:30 AM IST
Ahmedabad: Pharma major, Zydus Lifesciences Limited has received final approval from the United States Food and Drug Administration (USFDA)...
Johnson and Johnson Gets CDSCO Panel Nod for Talqetamab in Relapsed Multiple Myeloma, Phase IV Trial Mandated

Johnson & Johnson gets CDSCO Panel for additional indication of Amivantamab Liquid Concentrate for Infusion

Dr. Divya Colin12 April 2025 5:45 AM IST
New Delhi: In a significant development, the drug major Johnson and Johnson has got the go-ahead from the Subject Expert Committee (SEC) functional...
Intas Pharma

Submit Phase III CT data with Pk and Pd data: CDSCO Panel Tells Intas Pharmaceuticals on Human von Willebrand Factor

Dr. Divya Colin12 April 2025 5:30 AM IST
New Delhi: In response to the proposal for the grant of permission to manufacture Human von Willebrand Factor EP 600 IU (Freeze Dried Powder) Drug...
Strides Pharma Science arm New York facility gets 4 USFDA observations

Aurobindo Pharma arm gets 11 USFDA observations for Raleigh Plant

Ruchika Sharma11 April 2025 5:46 PM IST
Hyderabad: Aurobindo Pharma has announced that the United States Food and Drug Administration (USFDA) has issued 11 observations after an...
Doctor, retired police officer duped of Rs 1.44 crore in fake investment scheme

Pharma Scam worth Rs 10 Cr in Ludhiana: Company Employees Booked for Massive Internal Fraud

Farhat Nasim11 April 2025 4:16 PM IST
Ludhiana: A major pharmaceutical company located in Ludhiana's Industrial Area A has become the latest victim of internal financial fraud, with losses...
USFDA plans to phase out animal testing requirement for monoclonal antibodies, other drugs

USFDA plans to phase out animal testing requirement for monoclonal antibodies, other drugs

Ruchika Sharma11 April 2025 4:08 PM IST
In a significant move toward modernizing drug development, the U.S. Food and Drug Administration (USFDA) has announced plans to phase out its...
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Evaluation of Biologic Efficacy and Cost per NNT in Moderate-to-Severe Psoriasis: Indian Analysis

Evaluation of Biologic Efficacy and Cost per NNT in Moderate-to-Severe Psoriasis: Indian Analysis

U.S. FDA Grants Approval for Ranitidine Comeback

U.S. FDA Grants Approval for Ranitidine Comeback

Dapagliflozin and Sitagliptin FDC in T2D with Heart Failure: 2025 Indian Practice Review

Dapagliflozin and Sitagliptin FDC in T2D with Heart Failure: 2025 Indian Practice Review

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Importance of Early Aggressive Glucose Control - Approach in 2026

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