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|April 2, 2020
- Pharmaceutical Technology-04-02-2020
- Volume 44
- Issue 4
Custom-Built Heated Storage Vessel
The 20,000-gallon storage vessel from Ross Engineering measures at 10.5-ft outer diameter x 30-ft. long and is designed for product storage under atmospheric pressure at 200 ºF; it is UL-142 rated.
The 20,000-gallon storage vessel from Ross Engineering measures at 10.5-ft outer diameter x 30-ft. long and is designed for product storage under atmospheric pressure at 200 ºF; it is UL-142 rated. The stainless-steel vessel comes equipped with a 32-in. manway with davit for easy access to an internally supported insertion heater, along with nozzles, saddles, and lugs as specified by the end user. The vessel is also blasted and painted with black primer for outdoor exposure.
Articles in this issue
over 6 years ago
Biosimilars Poised for Gains in US Marketover 6 years ago
Critical Knowledge for Preparing Auditsover 6 years ago
Can Vaccine Development Be Safely Accelerated?over 6 years ago
Supercritical Fluid Chromatography Systemover 6 years ago
Quaternary Diaphragm Pumpover 6 years ago
Well Plates and Cartridges for Liquid Extractionover 6 years ago
Alternative Cleaning Validation Methods for Biologicsover 6 years ago
Pharma’s Leadership Role in a PandemicRelated to this article
Christy Owings, Thermo Fisher, explains clinical trial supply chain risks in Latin America, importer-of-record strategy, AI, and eCOA delays.
PharmTech AI Pulse Check debuts: pharma experts tackle GxP 'slop,' multi-agent validation risk, OCR document mining, personalized mRNA cancer therapy.
Andrea K. Kerrigan, FDA, outlines how validation, data integrity, and QRM determine whether digital tools and AI strengthen or undermine CGMP compliance.
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.
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.