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|March 1, 2012
- Pharmaceutical Technology-03-01-2012
- Volume 2012 Supplement
- Issue 2
Pharmaceutical Technology March 2012 Solid Dosage Supplement (PDF)
Solid Dosage and Excipients
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Articles in this issue
over 14 years ago
The American National Standard for Excipient GMPover 14 years ago
Standardized Excipient GMPover 14 years ago
Powder Testing Techniques for Tablet Manufactureover 14 years ago
Meeting Solubility Challengesover 14 years ago
Advances in Taste-maskingover 14 years ago
Multilayer Tablets: Key Challenges and Trendsover 14 years ago
Physical-Chemical Identifiers: A Q&A with FDA on the Final GuidanceAdvertisement
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The recently opened NJ spray drying facility doubles capacity for amorphous solid dispersions, addressing solubility limits in roughly 70% of small-molecule pipelines.
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