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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

New Drug Application of Zydus Desidustat tablets by China Medical System Holdings accepted in China

Ruchika Sharma24 April 2024 3:02 PM IST

Discovered and developed by Zydus, Desidustat is being marketed by the group in India under the brand name Oxemia.

Dr Reddys Labs API Mirfield facility gets 7 USFDA observations

Dr Reddy's recalls six lots of Sapropterin Dihydrochloride Powder for Oral Solution 100 mg over sub potency

Ruchika Sharma24 April 2024 1:10 PM IST

Hyderabad, Princeton: Dr Reddy's Laboratories Ltd. has announced that it is voluntarily recalling six (6) lots of Sapropterin...

Lupin receives USFDA observations for two Pithampur manufacturing Units

USFDA issues EIR for Lupin Aurangabad facility

Ruchika Sharma24 April 2024 11:46 AM IST

Mumbai: Global pharma major Lupin Limited has announced that it has received the Establishment Inspection Report (EIR) from the United States...

Merck, Daiichi Sankyo Ifinatamab deruxtecan granted Breakthrough Therapy Designation by USFDA for pretreated extensive-stage small cell lung cancer

Merck gets Canadian nod for Keytruda in combo with fluoropyrimidine- and platinum-containing-chemotherapy for HER2-negative gastric or gastroesophageal junction adenocarcinoma

Ruchika Sharma23 April 2024 3:08 PM IST

Kirkland: Merck, known as MSD outside the United States and Canada, has announced that Health Canada has granted approval of KEYTRUDA...

Novartis to buy Tourmaline Bio for USD 1.4 billion

Eli Lilly buys new injectable medicine manufacturing facility from Nexus Pharma

Ruchika Sharma23 April 2024 12:30 PM IST

Indianapolis: Eli Lilly and Company and Nexus Pharmaceuticals, LLC have announced a definitive agreement for Lilly to acquire a manufacturing...

Sandoz to acquire Just-Evotec Biologics EU SAS in-house development, manufacturing capabilities in France for USD 300 million

Sandoz confirms European Commission nod of Pyzchiva

Ruchika Sharma23 April 2024 11:54 AM IST

Basel: Sandoz has announced that the European Commission (EC) has granted marketing authorization for Pyzchiva (biosimilar ustekinumab) developed...

Zydus Lifesciences launches Mirabegron ER Tablets in US for overactive bladder treatment

Ruchika Sharma22 April 2024 2:47 PM IST

Mirabegron is indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency and urinary frequency.

Insufficient Efficacy, Safety Data: CDSCO Panel Rejects Zydus Phase III CT Waiver Request for Voclosporin

Zydus Lifesciences arm gets marketing nod for Nulibry from UK MHRA for MoCD Type A

Ruchika Sharma22 April 2024 2:08 PM IST

Ahmedabad: Zydus Lifesciences Ltd. has announced that its wholly-owned subsidiary Sentynl Therapeutics, Inc., has received marketing...

Lupin unveils Mirabegron ER tablets in US

Ruchika Sharma22 April 2024 12:09 PM IST

Mumbai: Global pharma major Lupin Limited has announced the launch of Mirabegron Extended-Release Tablets, 25 mg, in the United States, after...

Merck unveils all-in-one genetic stability assay to accelerate biosafety testing

Ruchika Sharma21 April 2024 5:37 PM IST

Germany: Merck, a science and technology company, has launched the all-in-one, validated genetic stability assay of its kind. The Aptegra CHO...

USFDA approves Takeda Gammagard liquid ERC for primary immunodeficiency

Takeda gets USFDA nod for Entyvio subcutaneous administration for Crohn's disease

Ruchika Sharma21 April 2024 10:00 AM IST

Osaka: Takeda has announced that the U.S. Food and Drug Administration (FDA) has approved ENTYVIO (vedolizumab) subcutaneous (SC)...

Roche receives EU CE mark for Contivue for neovascular age-related macular degeneration

Roche Alecensa gets USFDA nod for ALK-positive early-stage lung cancer

Ruchika Sharma20 April 2024 12:05 PM IST

Basel: Roche has announced that the U.S. Food and Drug Administration (FDA) has approved Alecensa (alectinib) for adjuvant treatment following...

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