The Leadership Summit will bring senior pharma executives together to discuss supply chain resilience, medicine security, and manufacturing capacity amid growing geopolitical fragmentation.
|Articles|November 1, 2012
- Pharmaceutical Technology-11-01-2012
- Volume 2012 Supplement
- Issue 6
Pharmaceutical Technology, Analytical Supplement 2012 (PDF)
Analytical and Bioanalytical Testing
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Articles in this issue
almost 14 years ago
Moisture Matters in Lyophilized Drug Productalmost 14 years ago
A Novel Process for Developing Fully Human Monoclonal Antibodiesalmost 14 years ago
Improving Technology Transferalmost 14 years ago
Analytical Applicationsalmost 14 years ago
Using a Systematic Approach to Select Critical Process Parametersalmost 14 years ago
Nuclear Magnetic Resonance as a Bioprocessing QbD ApplicationAdvertisement
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This week, the FDA opened applications for its Expedited IND Pilot, quality experts presented at the PDA/FDA Joint Regulatory Conference, and Hovione expanded its spray drying capacity.
Christy Owings, Thermo Fisher, explains clinical trial supply chain risks in Latin America, importer-of-record strategy, AI, and eCOA delays.
PharmTech AI Pulse Check debuts: pharma experts tackle GxP 'slop,' multi-agent validation risk, OCR document mining, personalized mRNA cancer therapy.
Andrea K. Kerrigan, FDA, outlines how validation, data integrity, and QRM determine whether digital tools and AI strengthen or undermine CGMP compliance.
PharmTech spoke with Tara Dougal, event director for pharma at Informa Markets, about trends impacting the pharmaceutical industry and how CPHI Milan is addressing these areas this year.
Andrew Parker, PhD, executive drug development consultant, Quotient Sciences, explains how AI is integrated into pharmaceutical development.
PDA/FDA 2026 session maps the GMP audit lifecycle, root cause to CAPA closure, plus a local vs. above-site decision framework and two case studies.
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