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|September 2, 2015
- Pharmaceutical Technology-09-02-2015
- Volume 39
- Issue 9
Pharmaceutical Technology, September 2015 Issue (PDF)
Click the title above to open the Pharmaceutical Technology September 2015 issue in an interactive PDF format.
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Articles in this issue
about 11 years ago
Generating Savings from Room Declassificationabout 11 years ago
Cleaning a Vial Filling Lineabout 11 years ago
Establishing Limits for Dermal Absorption of Elemental Impuritiesabout 11 years ago
A Matter of Tasteabout 11 years ago
CMOs Concerned With Cost of Single-Use Equipmentabout 11 years ago
Manufacturers Face Key Policy and Regulatory Challengesabout 11 years ago
Getting Flexible with Manufacturingabout 11 years ago
Computerized Systems Validationabout 11 years ago
Collaborating on GMP Inspectionsabout 11 years ago
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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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