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Tag: CDSCO

You Searched For "cdsco"
Eli Lilly Gets CDSCO Panel Nod to Study Lepodisiran

Eli Lilly Gets CDSCO Panel Nod to Study Lepodisiran

Dr. Divya Colin25 April 2024 6:00 PM IST
New Delhi: The drug major Eli Lilly has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
USFDA nod to Ipratropium Bromide Nasal Solution

Lupin Digital Health's Lyfe Platform gets Class C Medical Device license from CDSCO

Ruchika Sharma25 April 2024 4:23 PM IST
Mumbai: Lupin Digital Health, India's evidence-based cardiology Digital Therapeutics (DTx) platform, has announced that its Lyfe platform has...
GSK in breach for misleading prescription information on Omjjara: industry body

GSK Gets CDSCO Panel Nod to Study antimalarial drug Tafenoquine

Dr. Divya Colin24 April 2024 6:00 PM IST
New Delhi: The pharmaceutical major GSK has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
Zydus Lifesciences arm application for Menkes disease treatment gets USFDA priority review

Zydus Lifesciences Gets CDSCO Panel nod to study Bivalent Typhoid and Paratyphoid A Conjugate Vaccine

Dr. Divya Colin24 April 2024 5:15 PM IST
New Delhi: Reviewing the Phase I clinical trial protocol of the vaccine Bivalent Typhoid and Paratyphoid A Conjugate Vaccine, the Subject Expert...
Zydus Gets CDSCO Panel Nod To Manufacture Market Letermovir 240 mg, 480 mg Tablet

Zydus Gets CDSCO Panel Nod To Manufacture Market Letermovir 240 mg, 480 mg Tablet

Dr. Divya Colin23 April 2024 6:00 PM IST
New Delhi: The drug major Zydus has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
Sanofi Sarclisa combo gets Japanese nod newly diagnosed multiple myeloma

Submit post-marketing safety data of Belumosudil in Chronic graft versus host disease: CDSCO Panel Tells Sanofi

Dr. Divya Colin21 April 2024 6:00 PM IST
New Delhi: Responding to the proposal presented by the drug major Sanofi to import and market Belumosudil tablets 200 mg, the Subject Expert Committee...
Novartis to acquire kidney disease drug maker Regulus Therapeutics for up to 1.7 billion

Novartis Gets CDSCO Panel Nod to Study anti-cancer drug Ribociclib

Dr. Divya Colin21 April 2024 5:30 PM IST
New Delhi: The drug major Novartis has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
Eli Lilly announces transitions in executive leadership

CDSCO Panel Approves Eli Lilly's protocol amendment proposal for Adjuvant Imlunestrant vs Standard Adjuvant study

Dr. Divya Colin21 April 2024 5:15 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has approved the drug major Eli...
As Ozempic, Wegovy Take Priority, Novo Nordisk Winds Down Insulin Portfolio In India

Novo Nordisk Gets CDSCO Panel Nod to Study new medicine NNC0519-0130

Dr. Divya Colin21 April 2024 5:00 PM IST
New Delhi: The drug major Novo Nordisk has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
Open to expand US manufacturing as tariff threat looms: Dr Reddys Labs

Dr Reddy's Laboratories gets CDSCO Panel Nod To Import and Market Toripalimab 240mg solution for infusion

Dr. Divya Colin20 April 2024 6:00 PM IST
New Delhi: Noting an unmet medical need for recurrent locally advanced/metastatic nasopharyngeal carcinoma (RM-NPC) in India, the Subject Expert...
CDSCO panel approval to Ursodeoxycholic acid

CDSCO approves Abbott's proposal for Protocol Amendment of Triamcinolone Hexacetonide study

Dr. Divya Colin20 April 2024 6:00 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has approved the protocol...
Conduct Phase III clinical trial: CDSCO Panel Tells BDR Pharmaceutical on Anti-cancer Drug Abiraterone Acetate

Conduct Phase III clinical trial: CDSCO Panel Tells BDR Pharmaceutical on Anti-cancer Drug Abiraterone Acetate

Dr. Divya Colin20 April 2024 5:45 PM IST
New Delhi: Reviewing the justification for waiver of the Phase III clinical trial of the anti-cancer drug Abiraterone Acetate presented by BDR...
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