This article describes the Specification for Round container with cap (1000 ml). which is used pack the Tablets. Specification for Round container with cap (1000 ml). I. Product Information: Supplier / Manufacturer : As...
This Document describes (Standard Operating procedure) SOP on procedure for carrying out Hold time study for material, accessories and equipment. SOP ON HOLD TIME STUDY OBJECTIVE: To lay down the procedure for carrying out...
This Document describes (Standard Operating procedure) SOP for procedure for handling of audits. SOP for Handling of Audits OBJECTIVE : To lay down the procedure for handling of quality audits. SCOPE This procedure is...
This Document describes (Standard Operating procedure) SOP for procedure for responsibilities of all functional department & individuals job description SOP on JOB Description OBJECTIVE : To lay down the procedure for responsibilities of all...
This Document describes (Standard Operating procedure) SOP for Operation, Maintenance and Cleaning of Bio Safety Cabinet. SOP for Operation, Maintenance and Cleaning of Bio Safety Cabinet OBJECTIVE : To lay down the procedure for operation,...
This Document describes (Standard Operating procedure) SOP for media fill operation in the sterile dry powder filling area to evaluate the capability of the aseptic process to produce sterile product. SOP ON MEDIA FILL OBJECTIVE...
This Document describes (Standard Operating procedure) SOP for hold time study for establishment of hold time of products at various stages such as lubricated granules / blend, compressed tablets, coated tablets and filled capsules,...
This Document describes (Standard Operating procedure) SOP for Measures Taken during carrying out process validation of drug products. I. Purpose & Scope: The Purpose of this SOP is to lay down the procedure for...
This article describes about Operation and calibration of Micropipettes using in Quality control microbiology department of pharmaceutical industry. SOP for operation and calibration of micropipettes. OBJECTIVE : To lay down the procedure for operation...
This article contains Quality Risk Assessment for PPM and HVAC filter cleaning activity. Quality Risk Assessment (QRA) for risks associated with PPM & filter cleaning activity of HVAC system. Quality Risk Assessment for PPM...
