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Allison Radwick on Muck Rack

Allison Radwick

As seen in: Bioprocess Online, Outsourced Pharma, Biosimilar Development
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Articles by Allison Radwick

05.30.24 -- 7 Bioprocess Intensification Strategies

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By Matthew Pillar Verified, Lucy Cook, Shawn Opatka, Allison Radwick
| Bioprocess Online Verified
Webinar: Measuring Viral Vector Purity, Stability, and Physical Titer in Minutes — with Just One Tool Industry expert Dr. Laura Pala will highlight the advantages of macro mass photometry to characterize viral vector purity and stability, and help you understand how the KaritroMP can quickly assess the purity of AdV preparations, quantifying empty capsids and other impurities. Click here to learn more.
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04.19.24 -- Outsourcing Through An Industry-Government Battle

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By Louis Garguilo Verified, Allison Radwick, Yves Massicotte
| Outsourced Pharma
A PhRMA survey concludes 63% of member companies expect to shift at least some of their R&D investment away from small molecules as a result of the new legislation called the Inflation Reduction Act (IRA). But a lot of this movement has been ongoing for almost 20 years. So what's the real scene, as the industry and government are at loggerheads?
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04.18.24 -- Fine-Tuning Analytical Development Strategies For Every Phase

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By Beata Talar, G. Gellermann, Allison Radwick, Maria Löflund
| Biosimilar Development Verified
Get more biosimilar development insight with our FREE newsletter Newsletter | April 18, 2024 Four Steps To Identifying The CDMO Proposal Worth Signing Transparency and communication are essential to the success of a manufacturing partnership. If a CDMO is unwilling to have frank conversations during the proposal phase, that's likely a red flag. The right partner's team will help you make educated choices while ensuring quality, reasonable costs, and timeline efficiency.
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04.18.24 -- Process Development: Stuck In The Middle With You

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By Louis Garguilo Verified, Allison Radwick, Sungkeum Seo, Jeremy Weisshar
| Outsourced Pharma
The introduction of ICH Q14 to analytical procedure development provides guidance on the recommended approach to assay development and the justifications regulatory bodies require to demonstrate the development of a method. While applying an AQbD approach may require more upfront work, the advantages are a better understood and more robust method, with greater regulatory flexibility.
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