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.
|Articles|February 2, 2015
- Pharmaceutical Technology-02-02-2015
- Volume 39
- Issue 2
Radio Frequency Dryer Improves Efficiency
Radio Frequency’s Macrowave Dryers feature volumetric heating, moisture reduction, shortened dwell times, and keep temperature uniform throughout temperature-sensitive materials.
Radio Frequency’s Macrowave Dryers feature volumetric heating, moisture reduction as low as 200 PPM, shortened dwell times, and keep temperature uniform throughout temperature-sensitive materials. Bed depths up to six inches experience rapid drying, and with cost-efficiency in mind, the dryer can reduce labor and energy costs by 60%. The dryer is designed for conveyorized applications and features instant on/off power control.
Radio Frequency
Articles in this issue
over 11 years ago
Hiden Analytical Combination Spectrometer Increases Repeatabilityover 11 years ago
Ross Disperser Maintains Consistencyover 11 years ago
FANUC Robot Enhances Cycles Per Secondover 11 years ago
Preventing Tablet Tooling Problemsover 11 years ago
Chiral Resolution with and without Resolving Agentsover 11 years ago
FDA Sets Agenda for 2015 Guidance Developmentover 11 years ago
Cures Require Compromiseover 11 years ago
Ligand-Binding Assays and the Determination of Biosimilarityover 11 years ago
Labeling of Biosimilarsover 11 years ago
FDA Sets Policies to Enhance Drug Security and SafetyRelated to this article
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.
Lori Dingledine, QC Director Microbiological Control and GTIC Operations at Genentech, provided input on the regulations surrounding raw material manufacturing and use for ATMPs in a presentation at the 2026 PDA/FDA Joint Regulatory Conference.
FDA opens applications for its Expedited IND Pilot, pairing sponsors with qualified research institutions to test rolling CMC review ahead of first-in-human trials.
2026 approvals, clinical data, and licensing deals are advancing subcutaneous biologics, reducing patient burden, and reshaping biopharma drug strategy.
Karthik Iyer, Eli Lilly, details an AI system linking GMP findings, audits, and deviations for cited, inspection-ready regulatory intelligence.