The PharmTech team focused on its coverage of AAPS PharmSci 360 this week, conducting interviews with experts on a range of topics including formulation platforms, AI, amorphous solid dispersions, and animal studies.
|Articles|April 1, 2010
- Pharmaceutical Technology-04-02-2010
- Volume 34
- Issue 4
Pharmaceutical Technology, April 2010 Issue (PDF)
Spending More Or Less, And On What?
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Articles in this issue
over 16 years ago
Inside USP: USP Reaches 2500 Reference Standardsover 16 years ago
Tracking Solid-Dosage Equipmentover 16 years ago
Inside EDQM: The Role of the Pharmacopeia in a Globalized Worldover 16 years ago
More Questions than Answersover 16 years ago
Stay Current at INTERPHEXover 16 years ago
Unconventional Communicationover 16 years ago
The Effect of Overencapsulation on Disintegration and Dissolutionover 16 years ago
In the Spotlight April 2010over 16 years ago
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Subathra Ramamoorthy, Veranova, on when to escalate to structural elucidation and pair orthogonal techniques when characterizing an impurity.
Manish Baviskar, Hubot CDMO, on ALCOA++ data integrity, model version change control, continuous monitoring, and human sign-off.
The agreement between CDER and OII with allow for coordinated marketing application assessments and inspections.
Manish Baviskar, Hubot CDMO, explains which AI skills validation engineers need first and why AI model updates must go through GMP change control.
Ron Filler, Drug Development Consultants, explains how USP's 1074 revision brings human-relevant safety science to formulators and excipient makers.
Nitin Kumar Swarnakar, PhD, global application lab manager at BASF, talks about spray drying for drying amorphous solid dispersions and Raman spectroscopy’s role as a quantitative analytical tool.
Aleksandra Zuraw, senior veterinary pathologist at Charles River, discusses how chain of custody, good laboratory practice, quality control, and validation are applied to digital pathology data used in drug development.
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