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|October 1, 2019
- Pharmaceutical Technology-10-01-2019
- Volume 2019 Supplement
- Issue 5
Pharmaceutical Technology North America, APIs, Excipients, and Manufacturing 2019 Supplement (PDF)
Click the title above to open the Pharmaceutical Technology APIs, Excipients, and Manufacturing 2019 in an interactive PDF format.
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Articles in this issue
almost 7 years ago
How Excipient Type Influences Self-Emulsifying Drug Deliveryalmost 7 years ago
Advancements in Encapsulation Technologyalmost 7 years ago
Additives and Processing Aids in Pharmaceutical Excipientsalmost 7 years ago
Planning a Successful API Procurement Strategyalmost 7 years ago
Uncovering Hidden Risks in Solid-State API Propertiesalmost 7 years ago
Market Dynamics Drive the Agenda for CPhI WorldwideAdvertisement
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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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