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Tag: cdsco

You Searched For "cdsco"
Synokem Pharmaceuticals gets CDSCO panel nod to conduct phase III CT of FDC Salicylic Acid plus Luliconazole

Synokem Pharmaceuticals gets CDSCO panel nod to conduct phase III CT of FDC Salicylic Acid plus Luliconazole

Dr. Divya Colin22 Jan 2023 4:15 PM IST
New Delhi: Drug major, Synokem Pharmaceutical has got approval from the Subject Expert Panel (SEC) functional under the Central Drug Standard Control...
Eris Lifescience gets CDSCO panel nod to study FDC of Metoprolol Succinate, Dapagliflozin

Eris Lifescience gets CDSCO panel nod to study FDC of Metoprolol Succinate, Dapagliflozin

Dr. Divya Colin21 Jan 2023 4:30 PM IST
New Delhi: Directing to present bioequivalence (BE) study results in the Subject Expert Committee (SEC) before initiating the Phase III clinical...
Substandard Drugs Flagged Across Multiple States, Over 130 Batches Fail Quality Tests In April

CDSCO Drug Alert: 70 drug samples including GSK Betnovate C cream, Cipla's Junior Lanzol mentioned in the list

Susmita Roy21 Jan 2023 1:08 PM IST
New Delhi: In its latest drug safety alert, the apex drug regulatory body, Central Drugs Standard Control Organization (CDSCO) has flagged 70 medicine...
Centre to introduce research linked incentive scheme to cover RnD costs for biotech products: DCGI Dr V G Somani

Centre to introduce research linked incentive scheme to cover RnD costs for biotech products: DCGI Dr V G Somani

Ruchika Sharma21 Jan 2023 11:23 AM IST
Underscoring the importance of policy reforms, innovation, and research and development, he said the government has taken several initiatives to aid...
CDSCO Panel allows Cipla to waive  requirements for phase 4 study of tocilizumab inj for giant cell arthritis

CDSCO Panel allows Cipla to waive requirements for phase 4 study of tocilizumab inj for giant cell arthritis

Dr. Divya Colin19 Jan 2023 6:00 PM IST
New Delhi: Considering that Giant Cell Arthritis is very rare disease and there is challenge in recruitment of patients, the Subject Export Committee...
Sun Pharma, Philogen complete patient enrollment in Phase III trial for Soft Tissue Sarcoma

Sponsor should submit rescue management plan: CDSCO Panel Tells Sun Pharma Over Psoriasis Drug Tildrakizumab

Susmita Roy18 Jan 2023 6:00 PM IST
New Delhi: Granting the permission to conduct the proposed study of Tildrakizumab 100mg/ml, the Subject Expert Committee (SEC) functional under the...
Health Ministry shocker in RTI reply: CDSCO, ICMR admit to multiple side effects of Covid-19 jabs

Health Ministry shocker in RTI reply: CDSCO, ICMR admit to multiple side effects of Covid-19 jabs

Farhat Nasim17 Jan 2023 2:04 PM IST
New Delhi: In a shocking response to an RTI query, the Central Drugs Standard Control Organisation (CDSCO) and Indian Council of Medical Research...
COVID vaccine: DCGI approves market authorisation for Serum Institute Covovax as heterologous booster dose

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.
Laurus Labs Asked to Submit Justification, Data for Pediatric Darunavir-Ritonavir FDC Proposal

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...
Molbio Diagnostics unveils Truenat MTB-INH test for drug resistance in TB patients

Molbio Diagnostics unveils Truenat MTB-INH test for drug resistance in TB patients

Ruchika Sharma14 Jan 2023 3:20 PM IST
Truenat is a point-of-care, portable, battery-operated, IoT-enabled, multi-disease, Real-Time PCR platform with a sample-to-result time of less than 1...
SEC Approves Serums Salk Polio Vaccine for Commercial Use, Recommends Phase I Trial for 21-valent Pneumococcal Vaccine

CDSCO panel recommends market authorization for Covovax jab as heterologous booster dose

MD Bureau13 Jan 2023 3:21 PM IST
New Delhi: An expert panel of the central drugs regulatory authority is likely to take a decision on Wednesday on granting market authorisation to...
Marion Biotech production license suspended over cough syrups linked to Uzbek deaths, WHO issues alert

Marion Biotech production license suspended over cough syrups linked to Uzbek deaths, WHO issues alert

MD Bureau13 Jan 2023 2:15 PM IST
CDSCO had in December initiated a probe in connection with the death of 18 children in Uzbekistan allegedly linked to Marion Biotech's cough syrups...
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