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 18, 2011
Complete Plant Closure: High-End Pharma/API Equipment Available in UK
Live & Webcast Auction: Includes tanks, reactors, isolation equipment, boilers, air compressors, thermal oxidizers, and more. Constructed from stainless steel, glass lined, and hastelloy.
Advertisement
Live & Webcast Auction: 30 March at 10:00 (local time)
Complete Plant Closure: High-End Pharma/API Equipment Available in UK.Aesica Pharmaceuticals is closing its Enfield, UK facility, freeing up premium pharmaceutical/API assets for sale.
Inspections: 28 & 29 March from 10:00-16:00 (local time).
Bid on site or via webcast at EquipNet.com/Aesica.
Small sample of premium equipment available:
- Pfaudler Balfour Blue Glass Lined 4700 Litre Jacketed Double Cone Blending System
- Cogiem Laitermik Stainless Steel Pressure Filter Dryer 1.76 Sq Metres area
- Heinkel HF 800 1 Continuous Hastelloy 120 litre capacity Drum Centrifuge system
- Pfaudler Balfour Horizontal 72 cubic metres Glass Lined Chemical Storage Tank
- And much more
Visit EquipNet.com/Aesica
Advertisement
Related 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.
Advertisement
Advertisement