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.
|Articles|May 2, 2011
- Pharmaceutical Technology-05-02-2011
- Volume 35
- Issue 5
Pharmaceutical Technology, May 2011 Issue (PDF)
Up Close and Personal
Advertisement
Articles in this issue
over 15 years ago
Report from Hungaryover 15 years ago
INTERPHEX Innovationsover 15 years ago
Supply Chain Painover 15 years ago
In the Spotlight May 2011over 15 years ago
Up Close and Personalover 15 years ago
Gelatin Capsule Shell Cross-Linkingover 15 years ago
Q&A with Greg Irace,sanofi-aventisover 15 years ago
Pharmaceutical Excipients for Hot-Melt Extrusionover 15 years ago
Global Healthcare on the Ground: Roche Takes on Illnesses in LDCsover 15 years ago
Beyond MicronizationAdvertisement
Related to this article
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.
The recently opened NJ spray drying facility doubles capacity for amorphous solid dispersions, addressing solubility limits in roughly 70% of small-molecule pipelines.
Advertisement
Advertisement