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The imperative of fridge-free vaccines

European Pharmaceutical Review

Many of today’s vaccines are produced in ready-to-inject liquid formulations that must be kept cold to maintain stability. However, this greatly complicates both the worldwide distribution and stockpiling of vaccines and other drugs. A requisite cold chain has been designed and implemented to be uninterrupted from factory to patient.

Vaccines 111
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The unsustainability of clinical trials and need for transformative change

Pharmaceutical Technology

How will RFK Jr’s American dream for vaccines play out? According to a November 2024 GlobalData report, per-trial costs have risen steadily since 2014, with single country trials increasing by 2.9% To learn more about the solutions provided by Paradigm Health, download the document below. per year over this decade.

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ICH Q6B for Analytics

PharmaTech

A magnifying glass examining a vintage vaccine vial surrounded by four minimalistic chart icons, symbolizing healthcare, medicine, and analytics in the context of global health monitoring. While the document itself is a quarter of a century old at this point, it is laid out in such a way that relevancy is maintained. Easton, R.L.

Dosage 52
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Pharmaceutical Compounding Calculations, Part Two–Bulk Drugs

PharmaTech

It builds on drug calculations topics previously described (1), including guidance documents (2–5). FDA guidance documents illustrate labeling salt drugs and associated active moieties. FDA, USP Salt Policy (December 2014). 1, 2014 (accessed April 29, 2025). YouTube.com , Dec.

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Oxford Nanopore makes stellar debut on UK stock market

pharmaphorum

It also won a £113 million contract to provide rapid saliva-based COVID-19 testing services to the NHS, although that was ended early by the UK government in the summer as demand fell due to vaccinations. It may also use the cash injection for “in-licensing opportunities and potential acquisitions”, according to the document.

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Why are Post-Approval Pregnancy Studies Post-Marking Requirements Rather Than Post-Marketing Commitments?

FDA Law Blog: Biosimilars

To better understand FDA’s approach in classifying postmarketing pregnancy studies as PMRs or PMCs, we reviewed all postmarketing requirements (PMRs) and postmarketing commitments (PMCs) related to maternal and fetal outcomes in FDA’s PMR/PMC database for drugs approved in the ten-year period from January 2014 through December 2023.

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207 community hospital presidents and CEOs to know | 2025

Beckers Hospital Review

Hoey directed field hospital operations and oversaw a mass vaccination program that administered over 140,000 doses. Mr. Kleinhanzl has also championed the use of AI documentation tools like Dragon DAX and Dragon Co-Pilot to combat clinician burnout and enhance care delivery. During the pandemic, Ms.