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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

USFDA nod to Granules India postherpetic neuralgia drug Gabapentin

Ruchika Sharma29 March 2023 11:46 AM IST

The medicine is also indicated as adjunctive therapy in the treatment of partial-onset seizures, with and without secondary generalization, in adults...

Senores Pharma arm facility gets 3 USFDA observations

FDC Roha facility successfully concludes USFDA audit

Ruchika Sharma29 March 2023 10:00 AM IST

Mumbai: FDC has announced that the US Food and Drug Administration (USFDA) has successfully concluded the audit with no observations (Zero 483’s) at...

Novartis opens new radioligand therapy manufacturing facility in California

Novartis buoyed by trial success in early-stage breast cancer

Ruchika Sharma29 March 2023 9:15 AM IST

Frankfurt: Novartis's Kisqali breast cancer drug cut the risk of recurrence in women who were diagnosed at an early stage of the disease in a pivotal...

Biocon unveils Liraglutide for diabetes, obesity in Netherlands

Biocon Biologics bags 'ABEA : Bioprocessing Excellence in South Asia' Award

Ruchika Sharma28 March 2023 4:15 PM IST

Biocon Biologics was recognized as the winner as it garnered the maximum number of votes from among 70,000 biopharma professionals who participated in...

Sanofi Gets CDSCO Panel Nod to Update Prescribing Information for Xenpozyme

Diabetes drug: Sanofi gets marketing authorization from CDSCO for Soliqua

Ruchika Sharma28 March 2023 3:14 PM IST

Soliqua (10-40 and 30-60 prefilled pens) is a once-daily injectable combination drug containing insulin glargine 100 Units/ml, which is a long-acting...

Indian Immunologicals wins DCGI okay to manufacture Measles-Rubella vaccine

Ruchika Sharma28 March 2023 2:15 PM IST

This vaccine has been proven through extensive human clinical trials to be immunogenic and safe for people of 9 months to 49 years, it said.

Zydus Lifesciences secures USFDA approval for Doxepin Hydrochloride Capsules USP, 10 mg, 25 mg, 50 mg, 75 mg, 100 mg

Ruchika Sharma28 March 2023 1:15 PM IST

Ahmedabad: Zydus Lifesciences Limited has announced that the company has received final approval for Doxepin Hydrochloride Capsules USP, 10 mg, 25 mg,...

Morepen Medtech, Bimedical FZE to form JV company in India

Morepen Labs Baddi facility clears USFDA inspection without any adverse observation

Ruchika Sharma28 March 2023 12:38 PM IST

Gurugram: Morepen Labs has recently announced that the United States Food and Drug Administration (USFDA) has conducted an inspection of the API...

Caplin Steriles Secures USFDA Approval for Generic Methylprednisolone Injection

Zydus Lifesciences bags USFDA nod for Levothyroxine Sodium for Injection for myxedema coma treatment

Ruchika Sharma28 March 2023 11:42 AM IST

The drug will be manufactured at the group's injectable manufacturing facility at Jarod, near Vadodara, India.

Duty hiked: Imported X-ray machines to get costlier from April 1

Ruchika Sharma27 March 2023 5:45 PM IST

New Delhi: The government has hiked customs duty on import of X-ray machines and non-portable X-ray generators to 15 percent with effect from April 1....

Fortis Healthcare CEO Dr Ashutosh Raghuvanshi elected as new President of NATHEALTH

Ruchika Sharma27 March 2023 4:45 PM IST

Mr. Siddhartha Bhattacharya, Secretary General, NATHEALTH will continue to lead and head NATHEALTH secretariat.

Natco Pharma gets 7 USFDA observations for Kothur Pharma Division

Lupin pharmacovigilance group concludes USFDA inspection with no observations

Ruchika Sharma27 March 2023 3:45 PM IST

Mumbai: Global pharma major Lupin Limited has announced that the United States Food and Drug Administration (U.S. FDA) has completed a Post-marketing...

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