2026 approvals, clinical data, and licensing deals are advancing subcutaneous biologics, reducing patient burden, and reshaping biopharma drug strategy.
News|Articles|June 1, 2004
- Pharmaceutical Technology-06-01-2004
- Volume 2004 Supplement
- Issue 4
Added Functionality Excipients: An Answer to Challenging Formulations
Author(s)Ashish A. Joshi, PhD
Added functionality excipients facilitate the development of novel drug delivery methods and improve processing techniques.
Articles in this issue
over 22 years ago
Ion Exchange Resins Unique Solutions to Formulation Problemsover 22 years ago
New Developments in Spray-Dried Lactoseover 22 years ago
The Use of Acrylic Resins for Improved Aqueous Enteric CoatingRelated to this article
The agency issued a direct final rule that supports the use of innovative testing methods to limit the use of animals and maintain existing safety standards.
The FDA approves Inluriyo-Verzenio combo for ESR1-mutated breast cancer; EMBER-3 data double PFS, with supply chain and diagnostics implications for manufacturers.
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.
The recently opened NJ spray drying facility doubles capacity for amorphous solid dispersions, addressing solubility limits in roughly 70% of small-molecule pipelines.
Sanofi will transfer 20 mature medicines and three manufacturing sites to Cheplapharm for a 26.4% equity stake, closing by Q3 2027.
On PharmTech.com this week, coverage of upcoming events continued, experts continued to discuss the use of AI in pharma, and validation in oral solid dosage product production was emphasized.
Christy Owings, Thermo Fisher, on why early supply chain partnership and site visits prevent costly eCOA and clinical trial delays.
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