News about Drug Discovery & Development

Frontage Labs Expands Early-Phase Clinical Capabilities for Global Drug Development

Frontage Labs Expands Early-Phase Clinical Capabilities for Global Drug Development

Frontage's US operations are anchored by a modern 160?bed, 36,000?sq?ft phase-I clinical unit in Secaucus, New Jersey, designed to conduct large?scale phase-I and bioequivalence (BE) studies as well as radiolabeled human AME research.

Drug Discovery & Development | 31/01/2026 | By News Bureau

NanoMosaic Secures FDA AMT Designation for Nanoneedle Technology in AAV Gene Therapy Manufacturing

NanoMosaic Secures FDA AMT Designation for Nanoneedle Technology in AAV Gene Therapy Manufacturing

FDA’s CBER grants Advanced Manufacturing Technology designation to NanoMosaic’s Nanoneedle platform, enhancing regulatory engagement and streamlining quality control in AAV gene therapy production.

Drug Discovery & Development | 30/01/2026 | By News Bureau

Grail Submits Final PMA Module to FDA for Galleri Multi-Cancer Early Detection Test

Grail Submits Final PMA Module to FDA for Galleri Multi-Cancer Early Detection Test

Grail files the final Premarket Approval module with the FDA for its Breakthrough Device-designated Galleri test, supported by data from over 25,000 participants in PATHFINDER 2 and the NHS-Galleri trial.

Drug Discovery & Development | 30/01/2026 | By News Bureau

European Commission Expands Bracco's Vueway Approval to Infants and Neonates

European Commission Expands Bracco's Vueway Approval to Infants and Neonates

Bracco Imaging secures EU approval to extend Vueway’s use to infants and neonates, enhancing safe and effective MRI diagnostics for young patients.

Drug Discovery & Development | 28/01/2026 | By News Bureau

European Commission Expands GSK's RSV Vaccine Arexvy to Adults Aged 18 and Above

European Commission Expands GSK's RSV Vaccine Arexvy to Adults Aged 18 and Above

GSK’s RSV vaccine Arexvy receives European approval for adults aged 18 plus, marking a major expansion in protection against RSV-related respiratory illness across the region.

Drug Discovery & Development | 28/01/2026 | By News Bureau

FDA Clears Expanded Access Programme for StemCyte's RegeneCyte Therapy in Long covid Patients

FDA Clears Expanded Access Programme for StemCyte's RegeneCyte Therapy in Long covid Patients

The FDA has approved an Expanded Access programme for StemCyte’s RegeneCyte, enabling eligible Long covid patients to access the cord blood-based therapy amid ongoing clinical trials.

Drug Discovery & Development | 27/01/2026 | By News Bureau 105

ACON Launches FDA-Cleared Flowflex Plus 4-in-1 Home Test for RSV, Flu and Covid, Including Infants

ACON Launches FDA-Cleared Flowflex Plus 4-in-1 Home Test for RSV, Flu and Covid, Including Infants

Acon Laboratories has launched the first FDA-cleared 4-in-1 home test detecting RSV, Flu A, Flu B and Covid-19, approved for adults and children as young as six months.

Drug Discovery & Development | 27/01/2026 | By News Bureau 163

BD Launches Research Cloud 7.0 With AI-Powered Horizon Panel Maker to Advance Flow Cytometry Research

BD Launches Research Cloud 7.0 With AI-Powered Horizon Panel Maker to Advance Flow Cytometry Research

BD has launched Research Cloud 7.0 globally, introducing the AI-driven Horizon Panel Maker to automate panel design, streamline workflows and enhance data quality in immunology and cancer research.

Drug Discovery & Development | 27/01/2026 | By News Bureau

AGC Biologics' Milan Facility Supports Commercial Launch of Waskyra Gene Therapy After US FDA and EU Approval

AGC Biologics' Milan Facility Supports Commercial Launch of Waskyra Gene Therapy After US FDA and EU Approval

AGC Biologics’ Milan Cell and Gene Centre of Excellence will support the commercial rollout of Waskyra following US FDA and EU approvals, strengthening treatment options for patients with Wiskott-Aldrich syndrome.

Drug Discovery & Development | 22/01/2026 | By News Bureau

CDSCO Flags 167 Drug Samples as Substandard, Seven Found Spurious

CDSCO Flags 167 Drug Samples as Substandard, Seven Found Spurious

India’s drug regulator has identified 167 medicine samples that failed quality tests and classified seven additional samples as spurious during routine surveillance conducted in December. The findings were released as part of the Central Drugs Standard Control Organisation’s (CDSCO) monthly drug alert.

Drug Discovery & Development | 22/01/2026 | By Darshana

 
 

 

 

We use our own and third party cookies to produce statistical information and show you personalized advertising by analyzing your browsing, according to our COOKIES POLICY. If you continue visiting our Site, you accept its use.

More information: Privacy Policy

 pharmaindustrial-india.com - Professional magazine for pharma industry suppliers and lab technology - CEDRO members