Pharmabiz

PMI urges US FDA Advisory Committee to recommend authorizing ZYN as a modified risk tobacco product

PMI urges US FDA Advisory Committee to recommend authorizing ZYN as a modified risk tobacco product: Stamford, Connecticut Tuesday, January 27, 2026, 11:00 Hrs [IST] Experts from ...
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BD announces global commercial release of BD Research Cloud 7.0, to helps scientists advance immunology and cancer research with AI-powered insights and automation

BD announces global commercial release of BD Research Cloud 7.0, to helps scientists advance immunology and cancer research with AI-powered insights and automation: Franklin Lakes ...
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Flowflex introduces first US FDA-cleared 4-in-1 home test detecting RSV, Flu A/B and Covid for ages 6 months+

Flowflex introduces first US FDA-cleared 4-in-1 home test detecting RSV, Flu A/B and Covid for ages 6 months+: San Diego, California Tuesday, January 27, 2026, 09:00 Hrs [IST] ACO ...
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Pharma industry sees CDSCO’s new norm of 60% shelf life on exports as hurdle

Nandita Vijayasimha, Bengaluru Tuesday, January 27, 2026, 08:00 Hrs [IST] ...
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TNCDA lodges complaint with PMBI against violations by Jan Aushadhi Kendras in Tamil Nadu

TNCDA lodges complaint with PMBI against violations by Jan Aushadhi Kendras in Tamil Nadu: Peethaambaran Kunnathoor, Chennai Tuesday, January 27, 2026, 08:00 Hrs [IST] The Tamil N ...
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TNCDA alerts NPPA about counterfeit drug racket in Pondicherry & online trade malpractices

TNCDA alerts NPPA about counterfeit drug racket in Pondicherry & online trade malpractices: Peethaambaran Kunnathoor, Chennai Tuesday, January 27, 2026, 08:00 Hrs [IST] The Tamil ...
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FPME raises critical areas of delay in export consignments of medicines at ports

FPME raises critical areas of delay in export consignments of medicines at ports: Shardul Nautiyal, Mumbai Tuesday, January 27, 2026, 08:00 Hrs [IST] In order to enhance ease of d ...
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16 states and 6 UTs did not submit NSQ data in December to CDSCO

UTs did not submit NSQ data in December to CDSCO: Gireesh Babu, New Delhi Tuesday, January 27, 2026, 08:00 Hrs [IST] Even as the drug regulators in the country hav ...
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Parse Biosciences introduces workflow for immune repertoire and transcriptome analysis

Parse Biosciences, the leading provider of accessible and scalable single cell sequencing solutions, announced the launch of a fully integrated immune repertoire and whole transcriptome analysis ...
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IntraBio’s Aqneursa receives European Commission’s marketing approval for treatment of Niemann-Pick Type C disease

IntraBio Inc, a global biopharmaceutical company that develops and commercializes targeted therapies for rare and common neurological, neurodevelopmental and mitochondrial diseases, has announced that ...
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Kooth to provide mental health services through its Soluna platform for up to 100,000 students

Kooth to provide mental health services through its Soluna platform for up to 100,000 students: London Saturday, January 24, 2026, 18:00 Hrs [IST] Kooth, a global leader in digita ...
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Avacta Therapeutics receives US FDA clearance of investigational new drug application for FAP-Exd (AVA6103)

Avacta Therapeutics, a clinical stage biopharmaceutical company developing pre|CISION, a tumour-activated oncology delivery platform, has announced the US Food and Drug Administration (FDA) clearance ...