This SOP is applicable for Entry and exit procedure for Microbiology Laboratory in Quality Control Laboratory of pharmaceuticals formulation plant. Procedure: Microbiology laboratory-General Areas: Microbiology laboratory…
Schedule U describes the particulars to be shown in manufacturing record. Following details are included in Schedule U: PARTICULARS TO BE SHOWN IN MANUFACTURING RECORDS…
GMP:- GMPs define a quality system that manufacturers use as they build quality into their products. For example, approved drug products developed and produced…
1.0 OBJECTIVE : To laid down procedure for Microbiological assay for determining the potency of the drug. 2.0 SCOPE : This SOP…
1.0 OBJECTIVE : To laid down procedure for microbial limit test in for the estimation of the number of viable aerobic micro-organisms present…
1.0 OBJECTIVE : This procedure is laid down to explain the mode of operation & calibration of Digital Automatic Karl Fischer Titrator. (Make: VEEGO, MODEL…
1.0 OBJECTIVE To provide a procedure for determining the Leak test of packed material. 2.0 SCOPE This SOP covers the Leak test of packed…
1.0 OBJECTIVE: To laid down the procedure for operation of Liquid Particulate measuring system (PAMAS) 2.0 SCOPE: This procedure is applicable for measuring the particulate…
1.0 OBJECTIVE : To laid down the procedure for operation of Total Organic Carbon Analyser (Sievers-900). 2.0 SCOPE : This procedure is applicable to…
1.0 Objective To lay down the procedure for in process checks during liquid oral manufacturing and packing. 2.0 Scope This procedure is applicable for in…
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