by Dr. Yashashwini Reddy | 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 Dr. Yashashwini Reddy | Sep 3, 2024
Standard Operating Procedure (SOP) for the Acquisition, Application, and Storage of Primary Standards 1.0 Purpose: 1.1 The purpose of this SOP is to establish a systematic procedure for the Acquisition, Application, and Storage of Primary Standards within the Quality...
by Dr. Yashashwini Reddy | Aug 28, 2024
Why Magnetic rods are used in Cleaning Verification in Pharma If you see, some regulatory agencies keep strict limits on metal contamination in pharmaceutical products. This is a very good initiative as it improves the quality of the medicines we consume. Prevention...
by Dr. Yashashwini Reddy | Aug 26, 2024
In-process check during Inspection of Tablets by IPQA Personnel Inspection of tablets is done after the compression or coating step in the pharmaceutical industry. This inspection process is a country-specific requirement based on the regulatory requirements of the...
by Dr. Yashashwini Reddy | Aug 13, 2024
“Understanding Master Copy, Control Copy, and Obsolete Copy in the Pharmaceutical Industry” In the Pharmaceutical industry document issue is very important and every document is traceable and accountable in the form of master copy, control copy, and...
