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Latest Industry News - Page 531

Senores Pharma to acquire two products of USFDA approved ANDAs from Teva Pharma USA

AstraZeneca concludes acquisition of Neogene Therapeutics

Ruchika Sharma17 Jan 2023 1:15 PM IST
UK: AstraZeneca has completed the acquisition of Neogene Therapeutics Inc.. Neogene will operate as a wholly-owned subsidiary of AstraZeneca, with...
Roche unveils new PCR test to improve Vaginitis Diagnosis in countries following CE Mark

Roche gets European Commission nod for Xofluza to treat influenza in children aged one year and above

Ruchika Sharma17 Jan 2023 12:15 PM IST
Influenza is a serious infectious disease and represents a significant threat to public health.
Serum Institute Gets NPPA Nod to Discontinue Two Pack Sizes of Tetanus Toxoid Vaccine

COVID vaccine: DCGI approves market authorisation for Serum Institute Covovax as heterologous booster dose

Ruchika Sharma17 Jan 2023 11:14 AM IST
Covovax is manufactured through technology transfer from Novavax.
USFDA approves label update for Rybelsus allowing use as first-line option for adults with type 2 diabetes: Novo Nordisk

USFDA approves label update for Rybelsus allowing use as first-line option for adults with type 2 diabetes: Novo Nordisk

Ruchika Sharma16 Jan 2023 4:15 PM IST
Plainsboro: Novo Nordisk has announced that the U.S. Food and Drug Administration (FDA) has approved a label update for Rybelsus (semaglutide) tablets...
Lupin bags USFDA nod for Dolutegravir, Rilpivirine tablets to treat HIV infection

Lupin bags USFDA nod for Dolutegravir, Rilpivirine tablets to treat HIV infection

Ruchika Sharma16 Jan 2023 3:20 PM IST
Mumbai: Global pharma major Lupin Limited today announced that it has received tentative approval from the United States Food and Drug Administration...
Solara Active Pharma Sciences Mangalore facility successfully completes USFDA inspection

USFDA issues 3 observations for Granules India Gagillapur facility

Ruchika Sharma16 Jan 2023 2:30 PM IST
Hyderabad: Granules India has recently announced that US Food and Drug Administration (USFDA) has concluded Pre-Approval Inspection (PAI) with three...
Lupin Launches Epilepsy, Migraine Drug Topiramate XR in US, Targets USD 164 Million Market

Lupin gets 2 USFDA observations for Somerset facility

Ruchika Sharma16 Jan 2023 1:15 PM IST
Mumbai: Lupin has announced that the company has received two observations from the US Food and Drug Administration (USFDA) at the closure of...
Zydus Lifesciences arm bags USFDA okay for Major Depressive Disorder drug Levomilnacipran Extended-Release

Zydus Lifesciences arm bags USFDA okay for Major Depressive Disorder drug Levomilnacipran Extended-Release

Ruchika Sharma16 Jan 2023 12:15 PM IST
Ahmedabad: Zydus Lifesciences Limited’s (formerly known as Cadila Healthcare Limited) subsidiary Zydus Pharmaceuticals (USA) Inc. (Zydus) has...
NPPA Panel Rejects Dr Reddys Omez ODT Plea For Seperate Price, Finds No Therapeutic Edge

Dr Reddy's Labs acquires trademark rights of breast cancer drug from Pfizer

Ruchika Sharma16 Jan 2023 11:00 AM IST
The in-house product will be retailed in the Indian market at a reduction of 85% from the current MRP to increase affordability and access to...
Andhra Pradesh allotts 531.77 acres of land to Laurus Labs

Laurus Lab gets CDSCO panel nod to Manufacture, Market HIV drug Dolutegravir Sodium Oral Film

Dr. Divya Colin15 Jan 2023 5:00 PM IST
New Delhi: In line with the bioequivalence study data presented by drug maker Laurus Lab, the Subject Expert Committee (SEC) functional under the...
Cancer MedTech Gets Clarity: CDSCO Releases Final Oncology Device Risk Classification List

Budget FY24: AiMeD recommends increasing custom duty on import of Chinese medical devices

Ruchika Sharma15 Jan 2023 1:45 PM IST
Instead of 18 percent GST applicable on some medical Devices that are not luxury goods, the industry body recommended that the GST needs to be a flat...
Novartis opens new radioligand therapy manufacturing facility in California

EMA seeks to issue guidance on liver damage from Novartis gene therapy Zolgensma

Ruchika Sharma15 Jan 2023 12:15 PM IST
The drug won conditional EU approval during early 2020 and it costs more than $2 million per patient
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Editorial

ROBUST Study Released: One of the Largest Beta-Blocker KAP Study Captures Place of Beta Blockers in Indian Real-World Practice

ROBUST Study Released: One of the Largest Beta-Blocker KAP Study Captures Place of Beta Blockers in...

Obesity-Prediabetes Duo: Why Clinicians Must Intervene Early?

Obesity-Prediabetes Duo: Why Clinicians Must Intervene Early?

SURPASS-2- Tirzepatide vs Semaglutide in Type 2 Diabetes

SURPASS-2- Tirzepatide vs Semaglutide in Type 2 Diabetes

Efficacy and Safety of Dapagliflozin-Vildagliptin in Indian T2DM Patients with CV Risk Factors

Efficacy and Safety of Dapagliflozin-Vildagliptin in Indian T2DM Patients with CV Risk Factors

SURPASS-2: Superior HbA1c and Weight Reduction With Tirzepatide vs. Semaglutide

SURPASS-2: Superior HbA1c and Weight Reduction With Tirzepatide vs. Semaglutide

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Journal Club Today

MRI Study Maps Brain Growth Across the Perinatal Period

MRI Study Maps Brain Growth Across the Perinatal Period

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Health News Today

Health Bulletin 07/February/2026

Health Bulletin 07/February/2026

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