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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

Dr Reddys Labs API Mirfield facility gets 7 USFDA observations

Dr Reddy's Labs arm invests over Rs 2 lakh in Clean Renewable Energy KK 2A

Ruchika Sharma5 Aug 2024 2:00 PM IST

Hyderabad: Dr Reddy's Labs has announced that Aurigene Oncology Limited (''AOL'') (formerly, Aurigene Discovery Technologies Limited), a wholly-owned...

Mankind Pharma bags CDSCO nod to start Phase 1 trials of Autoimmune drug candidate

Mankind Pharma Vice Chairman Juneja says BSV acquisition to aid future growth of Company

Ruchika Sharma5 Aug 2024 11:30 AM IST

Mumbai: Rajeev Juneja, Vice Chairman and Managing Director of Mankind Pharma, has underscored the strategic significance of the company's recent...

Darzalex receives positive EMA Committee opinion for high-risk smouldering multiple myeloma: Janssen-Cilag International

EMA Committee recommends Rybrevant in combo with chemotherapy for adult patients with lung cancer after failure of prior therapy

Ruchika Sharma4 Aug 2024 11:00 AM IST

Beerse: Janssen-Cilag International NV, a Johnson & Johnson company, has announced that the Committee for Medicinal Products for Human Use...

Zydus Wellness registers 20 percent net sales growth in Q1

Ruchika Sharma4 Aug 2024 10:00 AM IST

Ahmedabad: For the first quarter ended June 30, 2024, Zydus Wellness Ltd., recorded its highest ever Q1 net sales growth of 20 percent which...

USFDA concludes inspection at Zydus Lifesciences SEZ II, Ahmedabad plant

Gland Pharma gets 3 USFDA observations for Pashamylaram facility

Ruchika Sharma3 Aug 2024 4:18 PM IST

Hyderabad: Gland Pharma has announced that the United States Food and Drug Administration (US FDA) has concluded an inspection of the...

Bharat Biotech credited ICMR, NIV as Covaxin co-inventors after missing them initially: JP Nadda

Ruchika Sharma3 Aug 2024 3:05 PM IST

New Delhi: Union health minister J P Nadda revealed on Friday that the Indian Council of Medical Research (ICMR) and the National Institute of...

CDSCO along with State Drugs Controllers conducted risk-based inspections of 400 premises including MSMEs: JP Nadda

Ruchika Sharma3 Aug 2024 2:00 PM IST

New Delhi: In order to assess the regulatory compliance of drug manufacturing premises in the country, the Central Drugs Standard Control Organization...

Jubilant Pharmova to sell API business to wholly owned arm

DoP is implementing PLI Scheme for Pharma with total financial outlay of Rs 15,000 crore: MoS for Chemicals and Fertilizers

Ruchika Sharma3 Aug 2024 11:30 AM IST

New Delhi: The Department of Pharmaceuticals is implementing the Production Linked Incentive (PLI) Scheme for Pharmaceuticals with a total...

Marksans Pharma gets USFDA nod for heartburn drug

Marksans Pharma arm gets UK MHRA marketing authorization for oral emergency contraceptive pill

Ruchika Sharma2 Aug 2024 1:30 PM IST

Mumbai: Marksans Pharma Limited has announced that its wholly owned subsidiary Relonchem Limited has received Marketing Authorization for the...

USFDA approves Caplin Steriles Milrinone Lactate in 5% Dextrose Injection, Infusion bags

Alembic Pharma bags USFDA final nod for cancer injection Nelarabine

Ruchika Sharma2 Aug 2024 12:30 PM IST

Vadodara: Alembic Pharmaceuticals Limited today announced that the Company has received final approval from the US Food & Drug...

JnJ gets USFDA nod for Darzalex Faspro-based quadruplet regimen for newly diagnosed multiple myeloma who are transplant-eligible

Ruchika Sharma2 Aug 2024 11:30 AM IST

Horsham: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has approved DARZALEX FASPRO (daratumumab and...

CDSCO Panel Approves GSKs Proposal to Double Indian Patient Pool in Dostarlimab Trial

US FDA expands Jemperli plus chemotherapy approval to all adult patients with primary advanced or recurrent endometrial cancer: GSK

Ruchika Sharma2 Aug 2024 10:00 AM IST

London: GSK plc has announced the US Food and Drug Administration (FDA) has approved Jemperli (dostarlimab) in combination with carboplatin and...

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