Content on PharmTech.com this week ranged from fundamentals on the use of digital pathology in drug development, discussions on the use of AI in pharma, and regulatory actions impacting the industry.
|Articles|July 2, 2020
- Pharmaceutical Technology-07-02-2020
- Volume 44
- Issue 7
Pump Tubing System
AdvantaPure’s GORE STA-PURE Pump Tubing systems can now overmold into any manifold tubing assembly as its pump element.
AdvantaPure’s GORE STA-PURE Pump Tubing systems can now overmold into any manifold tubing assembly as its pump element. Designed for optimal performance in peristaltic pumps, the system is made with platinum-cured silicone rubber and ePTFE for a fluid transfer product that uses overmolding technology to provide a smooth contact surface for fluid flow.
The tubing system can also lessen the risk of tubing ruptures in pumps, withstand operating pressures up to 100 psig, maintain consistent flow rates, lower spallation, and support sterile fluid processing.
Articles in this issue
about 6 years ago
Qualification of a Swab-Sampling Procedure for Cleaning Validationabout 6 years ago
Performing Remote Audits During the Pandemicabout 6 years ago
Demand for Custom Dosage Forms Fuels Innovationabout 6 years ago
Learning Regulatory Lessons in Times of a Crisisabout 6 years ago
Business on Hold? EMA’s Full Recovery in Questionabout 6 years ago
Taking a Controlled Approachabout 6 years ago
Unprecedented Times in Vaccinesabout 6 years ago
No Business, Like Brexit Businessabout 6 years ago
Innovating Continuous Twin-Screw Granulation with Foam DeliveryRelated to this article
This article discusses risk-based lifecycle governance, system implementation considerations, and the progression of batch record control from paper-based to fully electronic systems.
Ronald Piervincenzi, USP, explains why manufacturers should act now and how benchmarking could reward reliable generic drug suppliers.
The FDA approves Lilly's once-weekly insulin efsitora for type 2 diabetes, raising Fc-fusion manufacturing, high-concentration pen, and capacity questions.
Florin Muraru, Gourav Pandey, and Richard Jaenisch explain where human sign-off belongs as multi-agent AI and document-parsing models reach GxP.
In this episode of Ask the Expert, Siegfried Schmitt, PhD, vice president, Technical at Parexel, and Susan J. Schniepp, distinguished fellow at Nelson Labs, discuss how companies should approach post-approval changes to their CMC regulatory filings.
The EC has approved AstraZeneca's Trixeo Aerosphere as the first single-inhaler triple-combination therapy for asthma in the EU, based on phase e data showing improved lung function and fewer severe exacerbations in patients uncontrolled on standard ICS/LABA treatment.
In this episode of Pharma Fundamentals, Dr. Aleksandra Zuraw, senior veterinary pathologist at Charles River, provides an introduction to the use of digital pathology in drug development.
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