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Latest Industry News - Page 194

Principal Scientific Adviser to GoI reviews progress to transform India regulatory ecosystem for medical products

Principal Scientific Adviser to GoI reviews progress to transform India regulatory ecosystem for medical products

Ruchika Sharma22 Aug 2024 11:30 AM IST
New Delhi: Prof. Ajay Kumar Sood, Principal Scientific Adviser (PSA) to the Government of India took a meeting to review the progress made...
Daiichi Sankyo, AstraZeneca Enhertu gets USFDA breakthrough therapy designation for certain patients with HER2 low or HER2 ultralow metastatic breast cancer

Daiichi Sankyo, AstraZeneca Enhertu gets USFDA breakthrough therapy designation for certain patients with HER2 low or HER2 ultralow metastatic breast cancer

Ruchika Sharma21 Aug 2024 3:37 PM IST
Tokyo: ENHERTU (fam-trastuzumab deruxtecan-nxki) has been granted Breakthrough Therapy Designation (BTD) in the U.S. for the treatment of unresectable...
AbbVie seeks USFDA nod for combination regimen of Venclexta, Acalabrutinib

JnJ chemotherapy free lung cancer treatment Rybrevant plus Lazcluze gets USFDA okay

Ruchika Sharma21 Aug 2024 12:30 PM IST
New Jersey: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has approved RYBREVANT (amivantamab-vmjw) plus...
CDSCO Panel Approves GSKs Proposal to Double Indian Patient Pool in Dostarlimab Trial

GSK secures USFDA Breakthrough Therapy Designation for GSK5764227 for extensive stage small cell lung cancer

Ruchika Sharma21 Aug 2024 11:30 AM IST
London: GSK plc has announced that the US Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation for GSK5764227 (GSK’227),...
Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

Johnson & Johnson to acquire V-Wave

Ruchika Sharma21 Aug 2024 10:00 AM IST
New Brunswick: Johnson & Johnson has announced that it has entered into a definitive agreement to acquire V-Wave Ltd., a privately-held...
Marksans Pharma gets USFDA nod for heartburn drug

USFDA issues EIR for Marksans Pharma Goa facility

Ruchika Sharma20 Aug 2024 4:45 PM IST
Mumbai: Marksans Pharma has announced that the US Food and Drug Administration (USFDA) has issued an Establishment Inspection Report (EIR) for...
Lupin bags USFDA approval for Multiple myeloma treatment

Granules India bags USFDA okay for Glycopyrrolate Oral Solution

Ruchika Sharma20 Aug 2024 3:39 PM IST
Hyderabad: Granules India has announced that the U.S. Food and Drug Administration (FDA) has approved its Abbreviated New Drug Application (ANDA)...
Aurobindo Pharma arm incorporates new wholly owned subsidiary in Malaysia

Aurobindo Pharma China plant expected to be commercialised from Q3 FY25: CFO

Ruchika Sharma20 Aug 2024 2:28 PM IST
New Delhi: Hyderabad-based pharmaceutical company, Aurobindo Pharma anticipates that its China facility will begin production in the upcoming...
Groundbreaking digital platforms, Indian Pharmacopoeia online portal, Adverse Drug Reaction Monitoring System software launched at First Policy Makers Forum

Groundbreaking digital platforms, Indian Pharmacopoeia online portal, Adverse Drug Reaction Monitoring System software launched at First Policy Makers' Forum

Ruchika Sharma20 Aug 2024 12:30 PM IST
New Delhi: Union Minister of Health and Family Welfare & Chemicals and Fertilizers, Shri J.P. Nadda inaugurated the 'First Policy Makers'...
Natco Pharma gets USFDA EIR for Kothur Pharma division

Strides Pharma Science arm gets USFDA EIR for Alathur facility

Ruchika Sharma20 Aug 2024 11:25 AM IST
Bengaluru: Strides Alathur Private Limited, a wholly-owned subsidiary of Strides Pharma Science Limited has received an Establishment Inspection...
AstraZeneca announces Rs 176 crore investments in India to expand Chennai GITC

CDSCO Panel Approves AstraZeneca's protocol amendment proposal for COPD drug Tozorakimab

Dr. Divya Colin19 Aug 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...
AstraZeneca Gets SEC Approval to Conduct Phase IV Trial of Hyperkalemia Drug Sodium Zirconium Cyclosilicate

AstraZeneca gets USD 107 million Pfizer verdict overturned in US cancer drug patent fight

Ruchika Sharma19 Aug 2024 4:45 PM IST
Cambridge: AstraZeneca has convinced a Delaware federal judge to throw out a jury's decision that the company owes USD 107.5 million for...
PrevNext

Editorial

Evidence-Based Recommendation by Indian Pediatric Experts on the Use of Acid-Reducing Medications in Children

Evidence-Based Recommendation by Indian Pediatric Experts on the Use of Acid-Reducing Medications in...

Beta-Blockers After MI in Patients with LVEF Above 40%: Findings of BETAMI-DANBLOCK Trial Presented at ESC Congress 2025

Beta-Blockers After MI in Patients with LVEF Above 40%: Findings of BETAMI-DANBLOCK Trial Presented...

Beta-blockers Reduce Death, MI, Heart Failure 25% in Mildly Reduced LVEF:  Latest Meta-Analysis Presented at ESC Congress 2025

Beta-blockers Reduce Death, MI, Heart Failure 25% in Mildly Reduced LVEF: Latest Meta-Analysis...

From Potential to Global Impact: Strengthening India’s Research Ecosystem through Capacity Building - Dr Prashant Mishra

From Potential to Global Impact: Strengthening India’s Research Ecosystem through Capacity Building...

Exploring Buccal Prochlorperazine: A Targeted Review of Its Pharmacological Profile

Exploring Buccal Prochlorperazine: A Targeted Review of Its Pharmacological Profile

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Journal Club Today

Evidence-Based Recommendation by Indian Pediatric Experts on the Use of Acid-Reducing Medications in Children

Evidence-Based Recommendation by Indian Pediatric Experts on the Use of Acid-Reducing Medications in...

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Health News Today

Health Bulletin 19/September/2025

Health Bulletin 19/September/2025

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