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  • CDSCO (Central Drugs...

CDSCO (Central Drugs Standard Control Organisation) News - Page 11

Mandatory Excipients Disclosure on Drug Labels from March 2026: Health Ministry

Health Ministry Notifies Cosmetics Rules 2025, Empowers States To Suspend Licences

Farhat Nasim2 Aug 2025 5:59 PM IST
New Delhi: The Ministry of Health and Family Welfare has notified the Cosmetics (Amendment) Rules, 2025, making several key changes to the Cosmetics...
Intas Pharma Told to Revise Phase I, III Pembrolizumab Trial Protocol

CDSCO Panel Accepts Phase I Trial Data for Intas' Denosumab Biosimilar

Parthika Patel2 Aug 2025 4:40 PM IST
New Delhi: The Subject Expert Committee (SEC) under the Analgesic and Rheumatology division of the Central Drugs Standard Control Organisation (CDSCO)...
Submit BE Raw Data, Interaction Study on Dapagliflozin-Rosuvastatin FDC: Expert Panel Tells Pure and Cure

CDSCO Panel Clears PURE & CURE's Sickle Cell Trial With Conditions On Sample Size, Sites

Parthika Patel1 Aug 2025 5:09 PM IST
New Delhi: PURE & CURE Healthcare Pvt. Ltd. has received a recommendation from the Subject Expert Committee (SEC) under the Central Drugs Standard...
After Cough Syrup Deaths, CDSCO Tightens Oversight on Drug Testing Compliance

Veeda Clinical Research Gets Expert Committee Nod To Conduct BA/BE Study Of Ibrutinib For Export

Dr. Divya Colin1 Aug 2025 9:45 AM IST
New Delhi: Veeda Clinical Research Limited got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
CDSCO Panel Withholds Nod for Syngenes Pegfilgrastim Trial, Seeks Additional Data

CDSCO Panel Withholds Nod for Syngene's Pegfilgrastim Trial, Seeks Additional Data

Parthika Patel31 July 2025 2:01 PM IST
New Delhi: The Subject Expert Committee under the Central Drugs Standard Control Organisation (CDSCO) has directed Syngene International Limited to...
Zydus Told To Conduct Phase III Trial in India for Lurbinectedin Injection, BE Study Waived

Zydus Told To Conduct Phase III Trial in India for Lurbinectedin Injection, BE Study Waived

Parthika Patel31 July 2025 1:49 PM IST
New Delhi: Zydus Lifesciences Limited has been directed to conduct a Phase III clinical trial in the Indian population for its proposed oncology drug...
Braille Labels, QR Code Voice Assistance on Drugs? CDSCO Seeks Stakeholder Comments

CDSCO Introduces QR Code System for Streamlined Visitor Entry

Parthika Patel30 July 2025 3:53 PM IST
New Delhi: The Central Drugs Standard Control Organisation (CDSCO) has launched a new QR code-based online appointment system to simplify the process...
Ranitidine Under Cancer Cloud: CDSCO Calls for Monitoring NDMA Levels, Shelf Life Cuts

Ranitidine Under Cancer Cloud: CDSCO Calls for Monitoring NDMA Levels, Shelf Life Cuts

Parthika Patel28 July 2025 6:27 PM IST
New Delhi: The Central Drugs Standard Control Organization (CDSCO), under the Directorate General of Health Services, has issued a directive to all...
Goa unveils lifesaving therapies pricing policy

Expert Committee Clears Ravenbhel to Begin Resmetirom Phase 3 Trial, Asks for BE Data First

Parthika Patel27 July 2025 4:00 PM IST
New Delhi: The Subject Expert Committee (SEC) under the Gastroenterology and Hepatology division of the Central Drugs Standard Control Organisation...
Troikaas Fast-Acting Paracetamol Shot Hits Regulatory Hurdle, CDSCO Panel Seeks More Data

Troikaa's Fast-Acting Paracetamol Shot Hits Regulatory Hurdle, CDSCO Panel Seeks More Data

Dr. Divya Colin27 July 2025 3:00 PM IST
New Delhi: The Subject Expert Committee (SEC) under the Central Drugs Standard Control Organisation (CDSCO) has asked Troikaa Pharmaceuticals Ltd. to...
CDSCO Panel Seeks Safety Data on 5% Lenalidomide TDS Before Clearing 8% Patch Trial

CDSCO Panel Seeks Safety Data on 5% Lenalidomide TDS Before Clearing 8% Patch Trial

Parthika Patel25 July 2025 4:38 PM IST
New Delhi: The Subject Expert Committee (SEC) under the Oncology division of the Central Drugs Standard Control Organisation (CDSCO) has not granted...
CDSCO Panel Approves Phase IV Protocol Amendment for Bristol-Myers Squibbs Mavacamten Study

CDSCO Panel Approves Phase IV Protocol Amendment for Bristol-Myers Squibb's Mavacamten Study

Parthika Patel24 July 2025 6:49 PM IST
New Delhi: The Subject Expert Committee (SEC) under the Cardiovascular division of the Central Drugs Standard Control Organisation (CDSCO) has...
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Indias Unique CV Risk Profile: How to Decode the Role of Aspirin?

India's Unique CV Risk Profile: How to Decode the Role of Aspirin?

Vildagliptin-Dapagliflozin FDC Effective in High CV Risk Indian T2DM Patients: Findings from Latest DAa-ViNCI Study

Vildagliptin-Dapagliflozin FDC Effective in High CV Risk Indian T2DM Patients: Findings from Latest...

Tirzepatide proves to be more effective than semaglutide- Results of Surmount 5 Trial

Tirzepatide proves to be more effective than semaglutide- Results of Surmount 5 Trial

Pneumococcal Vaccination in Hematological Malignancies (HM)-Indian Hematology Expert Consensus 2025

Pneumococcal Vaccination in Hematological Malignancies (HM)-Indian Hematology Expert Consensus 2025

Negligence vs Misconduct: Where Do Medical Councils Draw the Line?

Negligence vs Misconduct: Where Do Medical Councils Draw the Line?

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Genome Sequencing in Newborns May Identify Life-Threatening Disorders Missed by Traditional Tests: Study Shows

Genome Sequencing in Newborns May Identify Life-Threatening Disorders Missed by Traditional Tests:...

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Health Bulletin 11/October/2025

Health Bulletin 11/October/2025

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