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|February 2, 2011
- Pharmaceutical Technology-02-02-2011
- Volume 35
- Issue 2
Pharmaceutical Technology, February 2011 Issue (PDF)
Real Time Release Testing
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Articles in this issue
over 15 years ago
SMART Bioprocess Designover 15 years ago
Follow-Ons: The New Black?over 15 years ago
Real Time Release Testingover 15 years ago
Rogue Pharmaciesover 15 years ago
Evaluating Late-Stage Pipelines and Potentialover 15 years ago
In the Spotlight February 2011over 15 years ago
Report from Indiaover 15 years ago
Friend or Foe: Prescription Drug Reimportation in the USover 15 years ago
Q&A with Dan Klees, MagnetrolAdvertisement
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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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