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|December 2, 2016
- Pharmaceutical Technology-12-02-2016
- Volume 40
- Issue 12
Pharmaceutical Technology, December 2016 Issue (PDF)
Click the title above to open the Pharmaceutical Technology December 2016 issue in an interactive PDF format.
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Articles in this issue
almost 10 years ago
Options in Employee Trainingalmost 10 years ago
Biosimilars Supporting Contract Manufacturers’ Growthalmost 10 years ago
Airlocks for cGMP Facilitiesalmost 10 years ago
Evaluating Mixing in a Single-Use Bioprocessing Systemalmost 10 years ago
Shrink Banders for Labeling Applicationsalmost 10 years ago
Chromatograph Enables Fast Recovery of Target Compoundsalmost 10 years ago
Automated Microscope for Multimodal Imagingalmost 10 years ago
From Bitter to Sweet: Developing a User-Friendly Painkilleralmost 10 years ago
Nurturing the Relationship Between Industry and Regulatorsalmost 10 years ago
Getting involved with pharma standardsAdvertisement
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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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