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|August 2, 2021
- Pharmaceutical Technology, August 2021 Issue
- Volume 45
- Issue 8
Eco-Friendly Freezers
Author(s)Pharmaceutical Technology Editors
Eppendorf's CryoCubeF440 freezer has been redesigned to promote sustainability through various green features.
Eppendorf has redesigned the CryoCubeF440 ultra-low temperature freezer class to be more sustainable by improving performance and incorporating eco-friendly cooling liquids and insulation foam.
The new freezer saves up to 23% of power and offers 30% more space relative to previous models, the company reports. A temperature of -80° C can be reached in 200 minutes; energy consumption at this temperature is 6.8 KW/h per day.
The freezer holds up to 320 storage boxes and can be monitored by the VisioNize box through a connection to the VisioNize Lab Suite.
Articles in this issue
about 5 years ago
Putting the Patient at the Heart of Dosage Form Designabout 5 years ago
A Digital Supply Chain Helps Ensure API Qualityabout 5 years ago
Serialization: Reducing Counterfeit Drugs and Increasing Salesabout 5 years ago
Designing Incubators for Cell Therapy Manufacturingabout 5 years ago
Implementing Data Integrity Compliance in a GLP Test Facilityabout 5 years ago
Developing the Best Formulation Partnershipabout 5 years ago
Working Towards Zero Emissionsabout 5 years ago
FDA Prioritizes Vaccine Review and Process ImprovementsRelated 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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