PharmTech AI Pulse Check episode 2 covers AI data governance, API-gated journals, watermarking limits, and why attribution beats detection in GxP.
|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
The FDA opened an expedited IND pilot, tightened scrutiny of foreign trial data, and finalized a rule recognizing non-animal testing methods. In Europe, the EMA advanced pharmaceutical legislation reform, restricted 2 legacy products, and opened an injectable-iron safety review.
Novartis licenses Abogen's mRNA-encoded T-cell engager for autoimmune disease, raising scale-up questions for mRNA-lipid nanoparticle manufacturing.
Pharma manufacturing spent 90 years learning that producing correct outputs isn't the same as catching your own errors. AI has only learned the first.
Ron Scarboro, Azurity Pharmaceuticals, explains why real-world usability belongs at product definition and how post-launch feedback should guide drug formulation.
Ronald Piervincenzi, USP, explains why drug supply resilience needs a system approach, from procurement benchmarks to regulatory capacity building.
Gene manufacturing platforms, patient-centric formulations, contract services, packaging innovations, and sterile filling lines are in the spotlight at CPHI Milan 2026.
Ronald Piervincenzi, USP, explains why drug supply resilience needs a system approach, from procurement benchmarks to regulatory capacity building.