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|July 1, 2010
- Pharmaceutical Technology-07-02-2010
- Volume 34
- Issue 7
Pharmaceutical Technology, July 2010 Issue (PDF)
Multiparticulates in Controlled Release: Has Their Time Come?
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Articles in this issue
over 16 years ago
A Glass Actover 16 years ago
Exploring the Tools in Nanoparticle Analysisover 16 years ago
Statistical Solutions: On the Verge of Significance: Why 5%over 16 years ago
Top-to-Bottom Collaborationover 16 years ago
Q&A with Metrics' David Varleyover 16 years ago
Report from Indiaover 16 years ago
Comparison of Superdisintegrants in Orally Disintegrating Tabletsover 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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