Vibha Jawa, PhD, chief scientific officer at EpiVax, explains why the need for animal studies varies by modality and what it takes for organ-on-chip and other human-relevant models to replace these studies in IND-enabling toxicology work.
|Articles|January 2, 2020
- Pharmaceutical Technology-01-02-2020
- Volume 44
- Issue 1
Pharmaceutical Technology North America, January 2020 (PDF)
Click the title above to open the Pharmaceutical Technology January 2020 issue in an interactive PDF format.
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Articles in this issue
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Human-Centered Work: How Pharma Can Move to a Blame-Free Culturealmost 7 years ago
Public Opinion: Can Pharma Chart a New Course?almost 7 years ago
Pharma Regulation to be Shaped by Pricing and Production Issuesalmost 7 years ago
Can Policy Keep Pace with Science and Discoveries?almost 7 years ago
Production, Packaging, and Inspectionalmost 7 years ago
ReNu Single-Use Technology Cartridge Assembliesalmost 7 years ago
Sanitary Tumble Blenderalmost 7 years ago
Plastic Mixing Systemsalmost 7 years ago
US Maintains Lead in Drug Development Despite Fewer Approvals in 2019almost 7 years ago
Choices for Climbing the Career LadderAdvertisement
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Sanjay Konagurthu, PhD, senior director of Science and Innovation at Thermo Fisher Scientific, explains what teams need to do to ensure the usefulness of AI and what strides have been made with AI in regulatory submissions.
Pauric Bannigan, Intrepid Labs, explains where AI speeds formulation decisions, why data is the bottleneck, and how active learning trains models with far less data.
The new initiative aims to apply traceable AI and science to expand care worldwide by translating discovery into tools that accelerate drug development.
Sanjay Konagurthu, PhD, senior director, Science and Innovation at Thermo Fisher Scientific, provides an update on the progress of AI and machine learning used in drug delivery.
Stephanie Johnson, Pfizer, explains how off-platform triggers, single-owner risk registers, and traceable prior knowledge keep protein formulation programs on track.
Stephanie Johnson, Pfizer, discusses how platform formulations moved 2 Pfizer protein programs to IND in 8 months by redistributing, not removing risk.
Shubhajit Paul, a senior research fellow in Boehringer Ingelheim’s Department of Material Analytical Sciences, spoke with PharmTech at AAPS PharmSci 360 to explain how tabletability prediction can be improved for roller-compacted formulations.
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