USFDA nod in. ICICI Direct upgrades outlook—calls it a “shot in the arm.”
Zydus Lifesciences gets Class I acceptance for CUTX-101.
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Vitaegiss Wellness Hiring 2025 Vitaegiss Wellness Hiring 2025 for QC, QA, QC Micro, Engineering, Warehouse Department at Ahmedabad location. Sanand GIDC 2 #USFDA Approval/Gmp/UL approved. 1. Current Opening in Vitaegiss Wellness Hiring 2025 1) Officer / Sr. Officer - Q. C Chemical Total position :3 Qualification: B. sc / M. sc Experience: 01-04 Year 2) Manager - QA Experience: 6-8 year Qulification: B Pharma / M Pharma…

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Stallion Laboratories Walk-In Interview 2025 – USFDA OSD Pharma Jobs in Ahmedabad, QA, QC, Production Vacancies Stallion Laboratories Walk-In Interview 2025, USFDA OSD Pharma jobs in Ahmedabad, QA QC Production vacancies, pharma careers Gujarat – Attend interview on 04 Oct 2025 for immediate joining. 1. Walk In Interview Details : Stallion Laboratories Pvt. Ltd. is hiring experienced professionals for its USFDA OSD pharmaceutical formulation facility in Ahmedabad, Gujarat. The company is conducting a Walk-In Interview on 04 October 2025…

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Patients Fight for Access to BrainStorm’s ALS Drug After Expanded Access Data ‘Defy Logic’ Participants in trials of BrainStorm Cell Therapeutics' NurOwn filed a Citizens’ Petition with the FDA earlier this month seeking a new review of the stem cell therapy that was rejected in 2022 based ...

Moms filed Citizens Petition asking the #USFDA to approve #NurOwn after it helped their loved ones with ALS "live longer & live better"

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FDA Panel to weigh conflicting data on Rexulti-Zoloft combo for PTSD The US FDA’s upcoming advisory panel will assess whether one positive and one negative Phase III trial, plus exploratory data, support approval.

The US FDA’s upcoming advisory panel will assess whether one positive and one negative Phase III trial, plus exploratory data, support approval for Otsuka Pharmaceutical’s Rexulti and Viatris’ Zoloft combo therapy for PTSD.

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FDA Panel to weigh conflicting data on Rexulti-Zoloft combo for PTSD The US FDA’s upcoming advisory panel will assess whether one positive and one negative Phase III trial, plus exploratory data, support approval.

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