Conveying Systems for the Pharmaceutical Industry: Types and Selection Guide
On most oral solid dosage lines, the biggest source of powder exposure and batch-to-batch variability is not the granul...
On most oral solid dosage lines, the biggest source of powder exposure and batch-to-batch variability is not the granul...
At the end of a production shift, a thin film of active residue might remain inside a high-shear granulator. It is invi...
A tablet that performs flawlessly at laboratory scale does not always survive the move to commercial production. In mos...
Your development team has just received the toxicology report for a new oncology API. The occupational exposure limit (...
What is Amorphous Spray Dried Dispersion (ASDD)? Over 70% of new drug candidates fall into BCS Class II or IV — high pe...
In a typical oral solid dose, the active pharmaceutical ingredient (API) may constitute less than 2% of the total tablet...
What Are Pharmaceutical Containment Solutions? In 2026, over 30% of drugs in development are classified as potent or hi...
What Is Fluid Bed Granulation? A single batch of powder can move from blending to dried granules in under 90 minutes — ...
A single failed cleaning validation run can freeze an entire oral solid dosage line for weeks. The investigation rarely...
Understanding the Root Causes of Tablet Defects A single capping defect can trigger a full batch rejection, costing $50...
1. Defining the Design Basis: Product, Scale, and Regulatory Target A project team once spent eight months on a facilit...
In 2026, over 70% of oncology pipeline candidates are classified as high potent APIs (HPAPIs) — compounds with an occup...