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|October 2, 2011
- Pharmaceutical Technology-10-02-2011
- Volume 35
- Issue 10
Pharmaceutical Technology, October 2011 Issue (PDF)
Click the title above to open the Pharmaceutical Technology October 2011 issue in an interactive PDF format.
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Articles in this issue
about 15 years ago
Pfizer Outlines Its Supply Strategyabout 15 years ago
Biopharmaceuticals from Plan to Productionabout 15 years ago
Inside EDQM: Mass Serialization to Combat Counterfeit Drugsabout 15 years ago
Applying Dry Powder Coatingsabout 15 years ago
Biotech Venture Funding Slips Below 2010 Levelsabout 15 years ago
Single-use Technologies in Fill–Finish Operationsabout 15 years ago
Sustainability Outside the Boxabout 15 years ago
Managing Business Risks During a Merger or Acquisitionabout 15 years ago
Is Noncompliance Just Human Nature?Advertisement
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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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