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Quality Control Bolg
How to investigation and take CAPA ? Deviation, Lab incident, OOS
Why investigation? To identified error  Random error Impacts precision (Weight error dilution  error injection to injection error Example document error, document error [ note : Precision show random error which is not control for us] +- positive and negative error...
(621) USP CHAPTER FOR CHROMATOGRAPHY
All chapter are use full for ADJUSTMENT of chromatography, TLC etc In such case some questions arias that Why adjustment in chromatography ? How adjustment justified ? Adjust chromatography If your method is validated and method are submitted in DMF so...
ALCOA to ALCOA Plus Plus for Data Integrity in pharma guideline
-Attributable,- Legible, – Contemporaneous,- Original,- Accurate, – Complete, – Consistent,- Enduring, – Available and data integrity topic
How can read Protocol analyst wet lab or Chemical analysis
â—‹ Whenever supervisor give work allocation for testing any product.â—‹ Then careful read specification(SOP) not missing any point which is defied in sopâ—‹ Before start analysis glassware collect in try â—‹ Labelling of each glassware â—‹ Seen availability chemicals and...
Analyst do some most common error ? How care and prevent QMS activity
Wet Lab analyst do Error ! Wet lab analyst are forgot a taken out of LOD or sulphated Ash, weight forgotten, etc ! . Some dilution error !. Weight print are not past in work sheet OR analytical work report or protocol etc (whatever terminology used). ! Calibration...
How can read Protocol analyst
HPLC Analyst â—‹ Whenever supervisor give work allocation for testing any product. â—‹ HPLC analyst first seen Test which is Assay by HPLC or RS By HPLC, Chiral test etc â—‹ Then careful read specification(SOP) not missing any point which is defied in sop â—‹ Then Seen Which...