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 2, 2011
- Pharmaceutical Technology-07-02-2011
- Volume 35
- Issue 7
Pharmaceutical Technology, July 2011 Issue (PDF)
Click the title above to open the Pharmaceutical Technology July 2011 issue in an interactive PDF format.
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Articles in this issue
over 15 years ago
PQRI Case Study (1): Defining Process Design Spaceover 15 years ago
FDA Introduces Spectral Libraryover 15 years ago
Biotech Financing Bluesover 15 years ago
All the Wrong Questionsover 15 years ago
In the Spotlight July 2011over 15 years ago
Pharma Leads in Sustainabilityover 15 years ago
Global Healthcare on the Ground: GlaxoSmithKline's Effortsover 15 years ago
In Search of an Optimal Solid Formover 15 years ago
Report from Europeover 15 years ago
FDA and Manufacturers Ponder Biosimilars PathwayAdvertisement
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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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