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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 [email protected] Contact no. 011-43720751

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Ruchika Sharma

Articles By : Ruchika Sharma

Bristol Myers Squibb Wins USFDA Approval for Opdivo Combo in Hodgkin Lymphoma

USFDA nod to Perioperative treatment of Neoadjuvant Opdivo, Chemotherapy followed by Surgery, Adjuvant Single Agent Opdivo for Resectable Non Small Cell Lung Cancer

Written By Ruchika Sharma5 Oct 2024 1:25 PM IST

Princeton: Bristol Myers Squibb has announced that the U.S. Food and Drug Administration (FDA) has approved Opdivo (nivolumab) for the...

Lupin arm buys nine brands of Medical Nutritional Institute in South Africa

Written By Ruchika Sharma5 Oct 2024 12:30 PM IST

The acquired brands include AntaGolin, RyChol, NeuroVance, SkinVance, FlamLeve, Rheumalin, SleepVance, ImmunoVance, and OviVance.

WHO unveils new guideline to improve global access to controlled medicines

FIRST: WHO approves Abbott Molecular mpox diagnostic test for emergency use

Written By Ruchika Sharma4 Oct 2024 1:39 PM IST

The World Health Organization (WHO) has listed the first mpox in vitro diagnostic (IVD) under its Emergency Use Listing (EUL)...

USFDA Approves Alembics Dapagliflozin Tablets, Grants 180-Day Exclusivity

Alembic Pharma gets USFDA nod for Alcaftadine Ophthalmic Solution

Written By Ruchika Sharma4 Oct 2024 11:30 AM IST

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

Caplin Steriles Secures USFDA Nod for Generic DEPO-MEDROL Injection

Indoco Remedies receives USFDA approval for allergy drug Cetirizine Hydrochloride

Written By Ruchika Sharma4 Oct 2024 9:00 AM IST

Mumbai: Indoco Remedies Limited has announced the receipt of final approval from the USFDA for Abbreviated New Drug Application (ANDA) for Cetirizine...

Indoco Remedies secures USFDA approval for Allopurinol Tablets to lower high uric acid levels in blood

Gilead Sciences inks pacts with Dr Reddy's Labs, Emcure, Hetero and 3 others for HIV drug Lenacapavir

Written By Ruchika Sharma3 Oct 2024 7:15 PM IST

Foster City: Gilead Sciences, Inc. has announced that it has signed non-exclusive, royalty-free voluntary licensing agreements with six pharmaceutical...

JnJ completes acquisition of Halda Therapeutics, its novel platform for cancer treatment

CCI approves acquisition of Bharat Serums and Vaccines by Mankind Pharma

Written By Ruchika Sharma3 Oct 2024 11:00 AM IST

New Delhi: Competition Commission of India has approved the acquisition of Bharat Serums and Vaccines Limited by Mankind Pharma Ltd. The proposed...

Language Row Costs Pharmacist: Action Ordered for Giving Wrong Medicine, Refusing Bengali

Zydus Lifesciences bags tentative USFDA nod for Enzalutamide Tablets for prostate cancer

Written By Ruchika Sharma2 Oct 2024 9:38 PM IST

Ahmedabad: Zydus Lifesciences Limited has received tentative approval from the United States Food and Drug Administration (USFDA) to manufacture...

After 40 Years, USFDA Approves Vanda Pharmas Motion Sickness Drug Nereus

USFDA nod to Aurobindo Pharma for Cephalexin Tablets

Written By Ruchika Sharma2 Oct 2024 8:00 PM IST

Hyderabad: Aurobindo Pharma Limited has announced that it has received final approval from the US Food & Drug Administration (USFDA) to...

Alkem Foundation, IIT Bombay collaborate to set up advanced research centre for immunotherapeutics, regenerative medicines

Lupin, Scope Ophthalmics Ireland ink pact to market Optase range of products in Mexico

Written By Ruchika Sharma2 Oct 2024 10:00 AM IST

Mumbai: Global pharma major Lupin Limited has announced that it has signed a distribution agreement with Scope Ophthalmics Ireland (SCOPE) for the...

Granules India packaging facility in US successfully completes USFDA inspection

USFDA issues EIR for Zydus Lifesciences Pharmez transdermal patch manufacturing facility

Written By Ruchika Sharma1 Oct 2024 4:22 PM IST

Ahmedabad: Zydus Lifesciences has received the EIR report from the U.S. Food and Drug Administration (USFDA) for the inspection conducted at its...

Mankind Pharma Gets Relief as CGST Appellate Authority Drops Rs 1.02 Cr Penalty

Mankind Pharma transfers OTC business to subsidiary Mankind Consumer Products

Written By Ruchika Sharma1 Oct 2024 3:03 PM IST

Mumbai: Mankind Pharma, a global pharmaceutical company, has executed a Business Transfer Agreement (BTA) to transfer its Over-the-Counter (OTC)...

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