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Ruchika Sharma

Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751

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Ruchika Sharma

Articles By : Ruchika Sharma

Cipla arm Medispray Goa facility classified as VAI by USFDA

Diabetes management: Cipla bags CDSCO regulatory nod for distribution, marketing of Afrezza (insulin human) Inhalation Powder in India

Ruchika Sharma12 Dec 2024 1:30 PM IST

Mumbai: Cipla Limited has announced that it has obtained regulatory approval from Central Drugs Standard Control Organisation (CDSCO) for the...

Biocon Biologics expands biosimilar insulin portfolio with USFDA nod of Kirsty

Biocon Biologics recognized as Asia IP Elite for 2024 by IAM

Ruchika Sharma12 Dec 2024 12:39 PM IST

Bengaluru: Biocon Biologics Limited, a subsidiary of Biocon Limited, has announced that it has once again been recognized as an Asia IP Elite for...

Merck Animal Health gets USFDA nod for Bravecto Quantum to protect dogs from fleas, ticks

USFDA nod to Gland Pharma Vitamin K deficiency treatment drug

Ruchika Sharma12 Dec 2024 11:26 AM IST

Hyderabad: Gland Pharma Limited, a generic injectable-focused pharmaceutical company, has received approval from the United States Food and Drug...

Phase 3 KEYLYNK-001 Trial Met Primary Endpoint of Progression-Free Survival in Patients With Advanced Epithelial Ovarian Cancer: Merck

Ruchika Sharma11 Dec 2024 5:54 PM IST

Rahway: Merck, known as MSD outside of the United States and Canada, has announced that the Phase 3 KEYLYNK-001 trial evaluating KEYTRUDA...

Alembic Pharma commissions new manufacturing facility in Pithampur to expand business

Alembic Pharma Panelav facility successfully completes ANVISA GMP audit

Ruchika Sharma11 Dec 2024 2:30 PM IST

Vadodara: Alembic Pharmaceuticals Limited has informed the exchange that the Company has successfully completed the Brazilian Health Regulatory...

$GSK Blenrep combos receive positive EMA Committee opinion in relapsed/refractory multiple myeloma$

Blenrep combo accepted for priority review in China in relapsed/refractory multiple myeloma: GSK

Ruchika Sharma11 Dec 2024 1:30 PM IST

London: GSK plc has announced that the National Medical Products Administration (NMPA) of China has accepted for review a new drug application...

Sanofi Rilzabrutinib earns orphan designation in EU for IgG4 related disease

Two Sanofi combination vaccine candidates for prevention of influenza, COVID gets USFDA Fast Track designation

Ruchika Sharma11 Dec 2024 12:25 PM IST

Paris: The US Food and Drug Administration (USFDA) has granted Fast Track designation to two Sanofi combination vaccine candidates to prevent...

USFDA accepts GSK submission for use of Nucala in COPD

Ruchika Sharma11 Dec 2024 11:30 AM IST

London: GSK plc has announced the US Food and Drug Administration (FDA) has accepted for review, data from the MATINEE study to support the...

Supriya Lifescience expands global footprint with Esketamine Hydrochloride approval, Atorvastatin patent filing

Ruchika Sharma11 Dec 2024 10:00 AM IST

Mumbai: Supriya Lifescience Ltd. has acquired approval from Brazil's health authority, ANVISA (Agência Nacional de Vigilância Sanitária), for...

Janssen-Cilag Guselkumab receives UK nod for Crohns disease, ulcerative colitis

CDSCO approves India's 1st robotic system SSI Mantra for telesurgery, teleproctoring

Ruchika Sharma10 Dec 2024 5:44 PM IST

New Delhi: Central Drugs Standard Control Organization (CDSCO) has given regulatory nod to the first Made-in-India SSI Mantra Surgical Robotic...

Karnataka govt forms panel to investigate maternal deaths in Ballari hospital

Ruchika Sharma10 Dec 2024 3:36 PM IST

Bengaluru: A four-member panel has been constituted by the Karnataka government to investigate maternal deaths reported at Ballari hospital and...

AbbVie seeks USFDA nod for combination regimen of Venclexta, Acalabrutinib

AstraZeneca-Daiichi Sankyo Datopotamab deruxtecan gets USFDA Breakthrough Therapy Designation for previously treated advanced EGFR-mutated non-small cell lung cancer

Ruchika Sharma10 Dec 2024 12:30 PM IST

Cambridge: AstraZeneca has announced that Datopotamab deruxtecan (Dato-DXd) has been granted Breakthrough Therapy Designation (BTD) in the...

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