The company is showcasing new development solutions and advanced digital technologies including its new OSD Express and Steriles Express solutions for drug development.
|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 Validationover 6 years ago
Performing Remote Audits During the Pandemicover 6 years ago
Demand for Custom Dosage Forms Fuels Innovationover 6 years ago
Learning Regulatory Lessons in Times of a Crisisover 6 years ago
Business on Hold? EMA’s Full Recovery in Questionover 6 years ago
Taking a Controlled Approachover 6 years ago
Unprecedented Times in Vaccinesover 6 years ago
No Business, Like Brexit Businessover 6 years ago
Innovating Continuous Twin-Screw Granulation with Foam DeliveryRelated to this article
Ron Scarboro, Azurity Pharmaceuticals, explains when formulation robustness justifies added cost and which post-approval quality and supply metrics teams can track.
The winners of the CPHI Pharma Awards 2026 include a neurodegeneration platform, a track-and-trace packaging innovation, a enzymatic mRNA manufacturing technology, and a cell-free enzymatic biomanufacturing platform.
Richard Jaenisch explains why NAMs are compressing drug development faster than AI and what FDA's new nonclinical testing rule means for sponsors.
Shadow AI and vendor data retention put GMP records and trade secrets at risk. AI Pulse Check panelists outline what pharma AI policies require.
Hovione's $35M CDC Flex line links spray drying to tablets, designed to eliminate scale-up under FDA Q13 guidance.
This week on PharmTech, Merck diversified its pipeline, USP emphasizes supply chain security, AI systems are examined, and speakers preview their presentations at CPHI Milan and AAPS PharmSci 360.
Capsugel's Bram Baert and Sandrine Picco argue that chasing zero nitrite in pharmaceutical excipients is often impractical and costly. They recommend setting scientifically justified, risk-based limits and consistently staying below them.