The PharmTech team focused on its coverage of AAPS PharmSci 360 this week, conducting interviews with experts on a range of topics including formulation platforms, AI, amorphous solid dispersions, and animal studies.
|Articles|January 2, 2017
- Pharmaceutical Technology-01-02-2017
- Volume 41
- Issue 1
Automatic Purge System for Control Panels
The Ross SysCon control panels can now be supplied with a fully automatic Type X Purge System, which forces clean air through the enclosure until all hazardous gases are removed.
The Ross SysCon control panels from Ross, Charles & Son can now be supplied with a fully automatic Type X Purge System, which forces clean air through the enclosure until all hazardous gases are removed. The system then maintains a slight positive pressure within the panel. The Type X Purge System includes a 24-volt power supply. The UL-listed Operator Stations are designed for use with a remote PLC System to ensure full operational functionality of the equipment they control.
Articles in this issue
almost 10 years ago
Predicting Moisture Uptake in Solid Dosage Packagingalmost 10 years ago
Blister Packaging Moves Forwardalmost 10 years ago
Staffing and Preparation for Auditsalmost 10 years ago
Fully Automated Capping Systemsalmost 10 years ago
Spray Dryer for Efficient Microencapsulationalmost 10 years ago
Vials Reduce Risk of Drug Container Interactionsalmost 10 years ago
The Tide Stays Highalmost 10 years ago
Drug Quality Key to Innovation and Accessalmost 10 years ago
FDA New Drug Approvals Down Significantly in 2016almost 10 years ago
Beyond Distractions, Pharma Moves OnRelated to this article
Subathra Ramamoorthy, Veranova, on when to escalate to structural elucidation and pair orthogonal techniques when characterizing an impurity.
Manish Baviskar, Hubot CDMO, on ALCOA++ data integrity, model version change control, continuous monitoring, and human sign-off.
The agreement between CDER and OII with allow for coordinated marketing application assessments and inspections.
Manish Baviskar, Hubot CDMO, explains which AI skills validation engineers need first and why AI model updates must go through GMP change control.
Ron Filler, Drug Development Consultants, explains how USP's 1074 revision brings human-relevant safety science to formulators and excipient makers.
Nitin Kumar Swarnakar, PhD, global application lab manager at BASF, talks about spray drying for drying amorphous solid dispersions and Raman spectroscopy’s role as a quantitative analytical tool.
Aleksandra Zuraw, senior veterinary pathologist at Charles River, discusses how chain of custody, good laboratory practice, quality control, and validation are applied to digital pathology data used in drug development.
Trending on Pharmaceutical Technology
1
AI Formulation: Regulators Want Data
2
AAPS PharmSci 360 2026: IND-Enabling Studies vs Animal Data
3
USP 1074 Revises Excipient Safety: AAPS PharmSci 360 2026
4
From URS to Acceptance Evidence: Defining and Testing Interfaces in Pen Injector Assembly
5