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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

Mounjaro, Wegovy sales in India double on month in July

Novo Nordisk Awiqli recommended for approval for diabetes by European regulatory authorities

Ruchika Sharma23 March 2024 2:12 PM IST

Awiqli is a once-weekly basal insulin analogue designed to cover the basal insulin requirements for a full week with a single subcutaneous injection.

USFDA approves Tonix Pharma Tonmya for fibromyalgia in adults

USFDA grants full approval for Abbvie Elahere for certain ovarian cancer patients

Ruchika Sharma23 March 2024 1:15 PM IST

North Chicago, Ill.: AbbVie has announced that the U.S. Food and Drug Administration (FDA) has granted full approval for ELAHERE...

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

JnJ gets USFDA nod for Opsynvi for chronic treatment of adults with pulmonary arterial hypertension

Ruchika Sharma23 March 2024 12:23 PM IST

Raritan: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has approved OPSYNVI - a single-tablet combination...

USFDA concludes audit at Cohance Lifesciences Jaggaiahpet facility

USFDA successfully concludes inspection at Neuland Labs Bonthapally facility

Ruchika Sharma22 March 2024 4:31 PM IST

Hyderabad: Neuland Laboratories Limited has announced that the United States Food and Drug Administration (US FDA) has successfully...

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

Bristol Myers Squibb Abecma approved in European Union for triple-class exposed relapsed and refractory multiple myeloma

Ruchika Sharma22 March 2024 4:02 PM IST

Princeton: Bristol Myers Squibb has announced that the European Commission (EC) has granted approval to Abecma (idecabtagene vicleucel;...

Takeda bags accelerated USFDA nod for Iclusig with chemotherapy in adult patients with newly diagnosed Ph+ ALL

Ruchika Sharma22 March 2024 11:57 AM IST

Osaka: Takeda has announced that the U.S. Food and Drug Administration (FDA) has approved the supplemental New Drug Application (sNDA) for...

Pfizer divests USD 3.5 billion stake in Haleon

Ruchika Sharma21 March 2024 2:10 PM IST

Sensodyne-marker Haleon has said that Pfizer, its top shareholder, divested approximately a $3.5 billion stake in the consumer healthcare firm,...

NPPA Panel Defers Biological Es Pneumonia Vaccine Price Exemption, Seeks Clarification

International Vaccine Institute begins technology transfer of Oral Cholera Vaccine to Biological E

Ruchika Sharma21 March 2024 12:48 PM IST

IVI will complete the technology transfer by 2025 and the oral cholera vaccine will be manufactured for India and international markets by Biological...

Bristol Myers Squibb concludes acquisition of Karuna Therapeutics

Ruchika Sharma21 March 2024 11:37 AM IST

Princeton: Bristol Myers Squibb has announced that the Company has successfully completed its acquisition of Karuna Therapeutics, Inc. With the...

Dr Reddys Labs API Mirfield facility gets 7 USFDA observations

Dr Reddys Labs unveils Versavo in UK for several types of cancers

Ruchika Sharma20 March 2024 2:30 PM IST

Hyderabad: Dr Reddy's Laboratories Ltd., a global pharmaceutical company, has announced the launch of Versavo (bevacizumab) in the United Kingdom...

Lupin schizophrenia drug Aripiprazole gets USFDA okay

Ruchika Sharma20 March 2024 1:30 PM IST

Aripiprazole Tablets USP are indicated for the treatment of schizophrenia, acute treatment of manic and mixed episodes associated with bipolar I...

USFDA nod to Johnson and Johnson EDURANT PED for certain pediatric patients living with HIV-1

Ruchika Sharma20 March 2024 12:30 PM IST

Titusville: Johnson & Johnson has announced that the U.S. Food and Drug Administration (FDA) has approved EDURANT PED (rilpivirine) for the...

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