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
Settle Plate Stand for Cleanrooms
Cherwell Laboratories expanded its line of stainless-steel prepared media accessories for cleanroom monitoring programs with its new floor standing settle plate stand.
Cherwell Laboratories expanded its line of stainless-steel prepared media accessories for cleanroom monitoring programs with its new floor standing settle plate stand. With the ability to hold one to two plates, the stand features a two-shelf design that has space for the exposed plate and its lid to prevent them from separating or getting damaged. The new model is floor standing and mounted on a single rod with a circular base for stability. Available at heights of 800mm and 1000mm, the stand can also be made to a customer-specified height.
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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