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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

Sanofi gets USFDA fast track designation for neovascular age-related macular degeneration gene therapy

Diabetes drug: Sanofi unveils Soliqua in India

Ruchika Sharma30 April 2024 2:35 PM IST

Soliqua is a once-daily injectable combination drug containing insulin glargine 100 Units/ml, which is a long-acting basal insulin and lixisenatide, a...

14 products of Baba Ramdev suspended by Indian State regulator: Report

Ruchika Sharma30 April 2024 1:30 PM IST

A recent report in Reuters stated that a state regulator in India has suspended the manufacturing licenses of 14 products produced by pharmaceutical...

Pfizer-Genmab gets full USFDA approval for Tivdak to treat recurrent or metastatic cervical cancer

Ruchika Sharma30 April 2024 12:30 PM IST

New York: Pfizer Inc. and Genmab A/S have announced the U.S. Food and Drug Administration (FDA) has approved the supplemental Biologics...

Granules India arm gets USFDA nod for Gout flares drug Colchicine

Ruchika Sharma30 April 2024 11:30 AM IST

Colchicine Capsules are indicated for prophylaxis of gout flares in adults.

Gland Pharma appoints Satnam Singh Loomba as COO, Senior Management Personnel

Ruchika Sharma29 April 2024 3:55 PM IST

Telangana: Gland Pharma has appointed Satnam Singh Loomba as Chief Operating Officer (COO); a Senior Management Personnel of the Company,...

Gland Pharma bags USFDA nod for Cangrelor for Injection

Gland Pharma bags USFDA nod for Cetrorelix Acetate for Injection

Ruchika Sharma29 April 2024 3:06 PM IST

Cetrorelix Acetate for Injection is used to prevent premature LH surges in women undergoing controlled ovarian stimulation.

One Death a Day: 1,705 Lives Lost in Indias Clinical Trials Since 2021, RTI Reveals

India becoming attractive for clinical trials: Pharma industry leaders

Ruchika Sharma29 April 2024 2:33 PM IST

New Delhi: Experts from the pharmaceutical sector have noted that over the last decade, clinical trials in India have undergone significant...

Vice President Dhankhar visits Bharat Biotech facilities at Hyderabad

Ruchika Sharma29 April 2024 12:13 PM IST

Hyderabad: The Honourable Vice President of India, Jagdeep Dhankhar has paid a visit to facilities of Bharat Biotech located at Genome Valley,...

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

JnJ gets positive CHMP opinion for Rybrevant, chemotherapy combo for first-line treatment of patients with advanced non-small cell lung cancer with activating EGFR exon 20 insertion mutations

Ruchika Sharma28 April 2024 12:30 PM IST

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

Gilead Seladelpar gets Conditional European Marketing Authorization for Primary Biliary Cholangitis treatment

USFDA approves Biktarvy label update with data for pregnant adults with HIV: Gilead Sciences

Ruchika Sharma28 April 2024 11:30 AM IST

Foster City: Gilead Sciences, Inc. has announced the U.S. Food and Drug Administration (FDA) has approved an updated label with additional data...

Bristol Myers Squibb, SystImmune gets USFDA Breakthrough Therapy Designation for izalontamab brengitecan for previously treated Advanced EGFR Mutated Non Small Cell Lung Cancer

EMA Committee recommends nod for Bristol Myers Squibb Opdivo in combination with Cisplatin, Gemcitabine for Urothelial Carcinoma

Ruchika Sharma28 April 2024 11:30 AM IST

Princeton: Bristol Myers Squibb has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines...

Medtronic gets USFDA nod for OmniaSecure defibrillation lead for placement within right ventricle

Medtronic gets USFDA approval for Inceptiv closed-loop spinal cord stimulator for chronic pain

Ruchika Sharma27 April 2024 4:59 PM IST

Dublin: Medtronic plc, a global leader in healthcare technology, has announced that the U.S. Food and Drug Administration (FDA) has approved the...

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