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  • Top Industry News

Top Industry News - Page 46

CDSCO Alert: 64 Drug Batches Including Metformin, Paracetamol Declared Not of Standard Quality in November

30 Formulations declared Not of Standard Quality as per data provided by states: CDSCO Drug Alert

Dr. Divya Colin24 July 2024 6:00 PM IST
New Delhi: In line with the 'Not of Standard Quality' data provided by states, the apex drug regulatory body, the Central Drug Standard Control...
NPPA Panel Defers Biological Es Pneumonia Vaccine Price Exemption, Seeks Clarification

Submit complete Phase-I CT report: CDSCO Panel Tells Biological E on Bivalent Typhoid and Paratyphoid A Conjugate Vaccine

Dr. Divya Colin23 July 2024 6:00 PM IST
New Delhi: Reviewing the interim Phase-I clinical trial report of Typhoid and Paratyphoid A Conjugate Vaccine Bivalent, the Subject Expert Committee...
CDSCO Alert: 64 Drug Batches Including Metformin, Paracetamol Declared Not of Standard Quality in November

CDCSO Declares 31 Formulations As Not of Standard Quality: Details

Dr. Divya Colin22 July 2024 6:00 PM IST
New Delhi: In its latest drug safety alert, the apex drug regulatory body, the Central Drug Standard Control Organisation (CDSCO), has flagged 31...
Conduct Phase III CT: CDSCO Panel Tells BDR Pharmaceuticals  on Linaclotide Capsules

Conduct Phase III CT: CDSCO Panel Tells BDR Pharmaceuticals on Linaclotide Capsules

Dr. Divya Colin21 July 2024 6:00 PM IST
New Delhi: Granting a waiver of the bioequivalence (BE) study, the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
Dr Reddys Labs secures European Commission approval for biosimilar to treat osteoporosis

Submit data on prevalence and genetic polymorphism of disease: CDSCO Panel Tells Dr Reddy's Laboratories on Siponimod tablet

Dr. Divya Colin20 July 2024 6:00 PM IST
New Delhi:In response to the proposal presented by the drug major Dr Reddy's Laboratories to manufacture and market the neurodrug Siponimod tablets...
Dr Reddys Labs secures European Commission approval for biosimilar to treat osteoporosis

Dr Reddy's Laboratories Gets CDSCO Panel Nod To Study Rebamipide, Sodium Alginate Suspension

Dr. Divya Colin19 July 2024 6:00 PM IST
New Delhi: The drug major Dr Reddy's Laboratories has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard...
Dr Reddys Labs secures European Commission approval for biosimilar to treat osteoporosis

Dr Reddy's Laboratories Gets CDSCO Panel Nod To Manufacture, Market Elobixibat Tablet

Dr. Divya Colin18 July 2024 6:00 PM IST
New Delhi: The drug major Dr Reddy's Laboratories has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard...
Ciplas Lanreotide Supply in US Hit After USFDA Observations at Pharmathen Facility

IT Department sends Rs 773 crore demand notice to Cipla

Ruchika Sharma17 July 2024 4:37 PM IST
Mumbai: Pharmaceutical giant Cipla has disclosed that it has received a demand notice amounting to Rs 773.44 crore from the Income Tax...
Cipla arm Medispray Goa facility classified as VAI by USFDA

Cipla Gets CDSCO Panel Nod to Study Plazomicin Injection

Dr. Divya Colin16 July 2024 6:00 PM IST
New Delhi: The drug major Cipla has got the go-ahead from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control...
Takeda announces closing of partnership with Innovent Biologics for oncology medicines

Submit Separate Retrospective, Prospective Study data of subjects: CDSCO Panel Tells Takeda on Velaglucerase alfa study

Dr. Divya Colin15 July 2024 6:00 PM IST
New Delhi: Regarding the post-marketing surveillance study of the drug major Takeda Pharmaceutical's Velaglucerase alfa injection, the Subject Expert...
Novartis concludes acquisition of Tourmaline Bio

CDSCO Panel approves Novartis Healthcare for selective use of Secukinumab dose up to 300 mg

Dr. Divya Colin14 July 2024 6:00 PM IST
New Delhi: Reviewing the justification presented by the drug major Novartis Healthcare for the monoclonal antibody Secukinumab, the Subject Expert...
Intas Pharma

Intas Pharmaceuticals Gets CDSCO Panel Nod for Palatability Study of Temozolomide powder for oral suspension

Dr. Divya Colin13 July 2024 6:00 PM IST
New Delhi: The drug major Intas Pharmaceuticals has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard...
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