Pharma Technology nominated as Trends Gazelle 2023
Pharma Technology has been once again nominated as Trends…
What are the advantages of external lubrication VS blending lubricant?
Introduction In this paper, we will analyze the advantages…
Another World "Première" for Pharma Technology !
The Brabant Walloon Chamber of Commerce & Industry brings…
Tablet and Capsule Visual Inspection
The T/CVIS-NSR Viswill inspection machines automatically inspect 360° of…
Pharma Technology in the Top 10 “Trends Gazelles 2020”
«I am proud to say that we have the…
Addressing Dust Accumulation in Tablet Manufacturing
Dedusting equipment and techniques address problems associated with tablet…
A Next-Generation approach to Quality Control in drug product development
Developing oral solid dosage (OSD) forms is complex. Traditional quality control methods often slow you down and increase risk. Our latest white paper reveals how CUB-X, a next-generation inspection system, transforms quality control with real-time, non-destructive analysis of critical quality attributes. Learn how to accelerate development, reduce waste, and ensure compliance from lab to production.
Formulation teams face challenges such as poor API solubility, limited early data, and slow detectability studies. Scaling up can expose hidden variability and increase regulatory demands for deeper process understanding. Relying on destructive, time-consuming methods adds cost and complexity, making real-time monitoring tools like Process Analytical Technology (PAT) essential for achieving Quality by Design (QbD).
Get access to the article by filling out the form below
|
|