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Dr. Kamal Kant Kohli
Dr. Kamal Kant Kohli

Dr Kamal Kant Kohli-MBBS, DTCD- a chest specialist with more than 30 years of practice and a flair for writing clinical articles, Dr Kamal Kant Kohli joined Medical Dialogues as a Chief Editor of Medical News. Besides writing articles, as an editor, he proofreads and verifies all the medical content published on Medical Dialogues including those coming from journals, studies,medical conferences,guidelines etc. Email: drkohli@medicaldialogues.in. Contact no. 011-43720751

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Articles By : Dr. Kamal Kant Kohli

Herpes Zoster Vaccine Linked to 50 Percent Drop in Shingles Among Inflammatory Arthritis Patients: Study

Herpes Zoster Vaccine Linked to 50 Percent Drop in Shingles Among Inflammatory Arthritis Patients: Study

Medha Baranwal15 Jun 2025 8:15 PM IST
USA: In a large real-world study, researchers have found that the Shingrix vaccine significantly reduces the incidence of shingles in individuals with...
Dupilumab Shows Promise as Novel Treatment for Necrobiosis Lipoidica: Case Report

Dupilumab Shows Promise as Novel Treatment for Necrobiosis Lipoidica: Case Report

Medha Baranwal15 Jun 2025 8:15 PM IST
USA: A recent case report published in The Open Dermatology Journal has brought attention to the successful use of dupilumab-a biologic commonly...
Merck in Talks to Acquire Revolution Medicines in USD 28-32 Billion Oncology Deal

Merck Keytruda approved by USFDA for Advanced Head and Neck Cancer

Ruchika Sharma15 Jun 2025 2:30 PM 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...
Dr Reddys Gets CDSCO Panel Nod To Import, Market Saccharomyces Boulardii, BE, CT Waived

Dr Reddy's Gets CDSCO Panel Nod To Import, Market Saccharomyces Boulardii, BE, CT Waived

Dr. Divya Colin15 Jun 2025 12:30 PM IST
New Delhi: Granting the bioequivalence study waiver and clinical trial study waiver, the Subject Expert Committee (SEC) functional under the Central...
Abbvie gets USFDA approval for updated indication statement for Rinvoq for Inflammatory Bowel Disease

USFDA approves expanded indication for AbbVie Mavyret for Acute Hepatitis C Virus

Ruchika Sharma15 Jun 2025 12:00 PM IST
North Chicago: AbbVie has received approval from the U.S. Food and Drug Administration (FDA) for a label expansion for MAVYRET...
AstraZeneca, Jacobio Pharma ink pact for proprietary Pan-KRAS inhibitor

AstraZeneca collaborates with CSPC Pharma focused on AI-enabled research

Ruchika Sharma15 Jun 2025 11:00 AM IST
Cambridge: AstraZeneca has entered a strategic research collaboration with Shijiazhuang City-based CSPC Pharmaceuticals Group Limited.Working...
NPPA Finally Allows GSK to Discontinue Grisovin FP

GSK RSV vaccine Arexvy accepted for regulatory review by EMA to expand use in adults 18 years, older

Ruchika Sharma15 Jun 2025 10:00 AM IST
London: GSK plc has announced that the European Medicines Agency (EMA) has accepted the company's regulatory application to expand the use...
Gufic Bioscience Told To Submit More Data for Piperacillin-Tazobactam-Sodium Chloride FDC

Gufic Bioscience Told To Submit More Data for Piperacillin-Tazobactam-Sodium Chloride FDC

Dr. Divya Colin15 Jun 2025 9:30 AM IST
New Delhi: In response to the proposal presented by Gufic Bioscience, the Subject Expert Committee (SEC) functional under the Central Drug Standard...
Abbott Volt Pulsed Field Ablation System bags USFDA approval for atrial fibrillation

SEC Asks Abbott to Submit More Data on Vitamin C Plus D3 FDC Chewable Tablet, Cites Lack of Justification

Dr. Divya Colin14 Jun 2025 6:19 PM IST
New Delhi: In response to the proposal presented by Abbott, the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
CDSCO Panel Accepts Mylans Post-Marketing Surveillance Report for Liposomal Amphotericin B Injection

CDSCO Panel Accepts Mylan's Post-Marketing Surveillance Report for Liposomal Amphotericin B Injection

Dr. Divya Colin14 Jun 2025 6:00 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has recommended to accept the...
Syngene International, Bristol Myers Squibb Extend Strategic Collaboration Through 2035

Syngene International Bengaluru facility successfully completes USFDA inspection

Ruchika Sharma14 Jun 2025 1:00 PM IST
Bengaluru: In a BSE filing, Syngene International has informed that the company's facility at Semicon Park, Bengaluru has successfully...
Sun Pharma Names Sana Shaikh as Head of Marketing

Sun Pharma gets 8 USFDA observations for Halol facility

Ruchika Sharma14 Jun 2025 11:05 AM IST
Mumbai: Sun Pharmaceutical Industries Limited has announced that US Food and Drugs Administartion (USFDA) has issued eight observations for its Halol...
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