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|February 1, 2018
- Pharmaceutical Technology-02-01-2018
- Volume 2018 Supplement
- Issue 1
Pharmaceutical Technology, 2018 Partnerships in Outsourcing Supplement (PDF)
Click the title above to open the Pharmaceutical Technology 2018 Partnerships in Outsourcing Supplement in an interactive PDF format.
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Articles in this issue
over 8 years ago
Bigger is Better in Samsung's Approach to Biomanufacturingover 8 years ago
Outsourcing Analytical Services in Early Drug Developmentover 8 years ago
Avoiding Complete Response Lettersover 8 years ago
A Three-Step Path Toward Combination Product Approvalover 8 years ago
Outsourcing: Does Focus Pay Off?over 8 years ago
Reducing Development Timelines and CostsAdvertisement
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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.
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