by Naveen kumar | Nov 24, 2024
Understanding Dirty Hold Time in Pharmaceutical Equipment Cleaning Dirty Hold Time (DHT) refers to the duration during which pharmaceutical equipment remains uncleaned after completing a manufacturing process. This period begins when the production ends and ends...
by Naveen kumar | Oct 13, 2024
Y Chute in Compression Machines: A Key to Efficient Tablet Production In pharmaceutical tablet manufacturing, precision and efficiency are crucial. One important component that contributes to these factors is the Y chute, a device used to manage the flow of granules...
by Naveen kumar | Sep 26, 2024
Understanding the Air Purge System in RMG: A Key to Pharmaceutical Safety In pharmaceutical manufacturing, maintaining cleanliness and preventing contamination is crucial. The air purge system in a Rapid Mixer Granulator (RMG) plays an essential role in ensuring...
by Naveen kumar | Sep 6, 2024
SOP For Operation of friability apparatus 1.0 OBJECTIVE To define the procedure for the operation and calibration of the friability test apparatus used in tablet testing. 2.0 SCOPE This Standard Operating Procedure (SOP) applies to the Production department. 3.0...
by Naveen kumar | Aug 29, 2024
“Essential Role of Desiccators in Pharmaceutical Stability and Quality Control” Introduction: A desiccator is a simple device made to keep the samples or materials in dry condition or simply it can also be considered a drying device, which picks up...
