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, 2013
- Pharmaceutical Technology-02-02-2013
- Volume 37
- Issue 2
Pharmaceutical Technology, February 2013 Issue (PDF)
Seeking Cold-Chain Efficiency
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Articles in this issue
over 13 years ago
Q&A With Chris Eclesover 13 years ago
Seeking Cold Chain Efficiencyover 13 years ago
The EU's Falsified Medicines Directive and APIsover 13 years ago
End of the Dedicated CMO?over 13 years ago
Offering a Pharma View of Social Mediaover 13 years ago
Tracking Growth in Biologicsover 13 years ago
Report from Indiaover 13 years ago
Rouge Contaminants and Water Systemsover 13 years ago
Pharma Conversation & Communityover 13 years ago
GMP Compliance Becomes Prominent Enforcement IssueAdvertisement
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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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