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Copyright Notice: This Article/SOP/Compilation/Published Content is protected by Indian & International Copyright Laws. Reproduction and Distribution of the same without written permission is prohibited. Mail us…
Copyright Notice: This Article/SOP/Compilation/Published Content is protected by Indian & International Copyright Laws. Reproduction and Distribution of the same without written permission is prohibited. Mail us…
PROTOCOL Requirements are as follows: a) Validation Team b) Objective c) Scope d) Responsibility e) Equipment description f) Operation Checks: i) Verify calibration of…
(A) Subjective: Procedure for performing Disintegration test. (B) Purpose: This procedure is applicable for performing dissolution test on drugs used in pharmaceutical company. (C) Name…
(A) Subjective: Procedure for performing Friability test on Tablets. (B) Purpose: This procedure is applicable for friability test on tablets and calibration of friabilator used…
Cleaning of Clean- Room Pass Boxes: (A) Subject: Procedure for Cleaning of Class- Room Pass Boxes. (B) Purpose: This procedure is applicable for Cleaning of Clean-…
(1) Dynamic Pass Box: Procedure on the working of Dynamic Pass Box. (A) Objective: This working principle is applicable for usage of Dynamic Pass Box in formulation…
A Clean- Room is an environment in which several parameters (like Contamination, Pressurization, Temperature & Humidity and Personnel Access) are controlled, monitored and maintained. Basically…
Below is a sortable listing of Pharmaceutical Quality/Manufacturing Standards (CGMP) Guidances CATEGORY TITLE Pharmaceutical Quality/Manufacturing Standards (CGMP) COMPRESSED MEDICAL GASES GUIDELINE Compliance; Pharmaceutical…
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