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Latest Industry News - Page 4

Natco Pharma gets 7 USFDA observations for Chennai facility

Natco Pharma gets 7 USFDA observations for Chennai facility

Ruchika Sharma21 Nov 2025 4:59 PM IST
Hyderabad: Natco Pharma has announced that the company has received seven observations from the U.S. Food and Drug Administration (FDA) after an...
No Trial Waiver: CDSCO Panel Directs Sun Pharma to Run Phase III Study for Somatropin Liquid Injection Citing Lack of India-Specific Data

No Trial Waiver: CDSCO Panel Directs Sun Pharma to Run Phase III Study for Somatropin Liquid Injection Citing Lack of India-Specific Data

Susmita Roy21 Nov 2025 4:26 PM IST
New Delhi: The Subject Expert Committee (SEC) under the Central Drugs Standard Control Organization (CDSCO) has opined that the drug major Sun...
AIIMS Not Obligated to Pay Stipend to Foreign PG Students: Delhi HC

Delhi HC Rejects FMC Plea, Clears Natco to Launch Cyantraniliprole Ahead of Patent Expiry

Susmita Roy21 Nov 2025 4:18 PM IST
New Delhi: Strengthening India's stance on fair market competition in agriculture, the Delhi High Court has denied FMC Corporation's attempt to...
Delhi Police Bust Rs 100-Crore Methamphetamine Cartel, Drug Kitchen, 4 Foreign Nationals Arrested

Delhi Police Bust Rs 100-Crore Methamphetamine Cartel, Drug Kitchen, 4 Foreign Nationals Arrested

Parthika Patel21 Nov 2025 4:16 PM IST
New Delhi: Acting on sustained surveillance and specific intelligence, the Delhi Police Special Cell has dismantled an international drug cartel,...
After Toxic Syrup Deaths, Govt Mulls Ending OTC Sale of Cough Syrups Nationwide

After Toxic Syrup Deaths, Govt Mulls Ending OTC Sale of Cough Syrups Nationwide

Parthika Patel21 Nov 2025 4:09 PM IST
New Delhi: India may soon restrict the sale of cough syrups strictly to doctor-prescribed use, as the Central Government is considering a major...
Pharmacies under fire: Over 2 lakh fake drugs seized, licences at risk in Kerala crackdown

Pharmacies under fire: Over 2 lakh fake drugs seized, licences at risk in Kerala crackdown

Ruchika Sharma21 Nov 2025 3:07 PM IST
Thiruvananthapuram: In a major crackdown on counterfeit medicines, Kerala's Drugs Intelligence Wing seized fake drugs worth over Rs two lakh...
GSK arm Tesaro initiates litigation against AnaptysBio

GSK arm Tesaro initiates litigation against AnaptysBio

Ruchika Sharma21 Nov 2025 2:15 PM IST
London: GSK subsidiary, TESARO, Inc., has initiated litigation against AnaptysBio, Inc. in the Delaware Chancery Court. This action contends that...
Bayer Hyrnuo secures USFDA accelerated approval for previously treated advanced HER2 mutant non small cell lung cancer

Bayer Hyrnuo secures USFDA accelerated approval for previously treated advanced HER2 mutant non small cell lung cancer

Ruchika Sharma21 Nov 2025 1:30 PM IST
Berlin: Bayer has received accelerated approval from the U.S. Food and Drug Administration (FDA) for HYRNUO (sevabertinib),for the treatment of...
India must move from being pharmacy of world to laboratory of world, says JP Nadda

India must move from being pharmacy of world to laboratory of world, says JP Nadda

Ruchika Sharma21 Nov 2025 12:30 PM IST
New Delhi: Union Minister of Health & Family Welfare and Chemicals & Fertilizers, J.P. Nadda, has called for reducing dependence on imported...
NPPA Panel Defers Biological Es Pneumonia Vaccine Price Exemption, Seeks Clarification

WHO grants Pre qualification status to Biological E 14-valent Pneumococcal Conjugate shot

Ruchika Sharma21 Nov 2025 11:30 AM IST
Hyderabad: Biological E. Limited, a Hyderabad-based vaccine and pharmaceutical company, has announced that the World Health Organisation...
Alexion, AstraZeneca Rare Disease Koselugo gets USFDA nod for neurofibromatosis type 1

Alexion, AstraZeneca Rare Disease Koselugo gets USFDA nod for neurofibromatosis type 1

Ruchika Sharma20 Nov 2025 5:00 PM IST
Alexion, AstraZeneca Rare Disease has received approval from the USFDA for Koselugo (selumetinib), an oral, selective MEK inhibitor for the...
Ocuvex Therapeutics resubmits Complete Response Letter to USFDA for PDP-716

Ocuvex Therapeutics resubmits Complete Response Letter to USFDA for PDP-716

Ruchika Sharma20 Nov 2025 4:14 PM IST
Mumbai: Sun Pharma Advanced Research Company Ltd. (SPARC) has announced that Ocuvex Therapeutics Inc. has resubmitted a Complete Response Letter...
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Real-World Evidence in Psoriatic Arthritis: PRO-SPIRIT Study

Real-World Evidence in Psoriatic Arthritis: PRO-SPIRIT Study

PRIME-Vilda Trial Results Highlights Vildagliptin SRs Efficacy and Safety in Indian Type 2 Diabetes Patients on Metformin

PRIME-Vilda Trial Results Highlights Vildagliptin SR's Efficacy and Safety in Indian Type 2 Diabetes...

Explainer Video: Acknowledge- Assisting Patients Through Challenges in Their Diabetes Care Journey

Explainer Video: Acknowledge- Assisting Patients Through Challenges in Their Diabetes Care Journey

Effect of Micronized Purified Flavonoid Fraction (MPFF) in Indian patients with Grade I-II Hemorrhoids: the IMPACT HD Study

Effect of Micronized Purified Flavonoid Fraction (MPFF) in Indian patients with Grade I-II...

Gliclazide - Revisiting a Preferred Sulphonylurea in 2025 - Dr Silima Tarenia and Dr Shehzad Ruman

Gliclazide - Revisiting a Preferred Sulphonylurea in 2025 - Dr Silima Tarenia and Dr Shehzad Ruman

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PRIME-Vilda Trial Results Highlights Vildagliptin SRs Efficacy and Safety in Indian Type 2 Diabetes Patients on Metformin

PRIME-Vilda Trial Results Highlights Vildagliptin SR's Efficacy and Safety in Indian Type 2 Diabetes...

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Health Bulletin 25/November/2025

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