by maheshbhuva | Mar 9, 2023 | stability
Stability studies are mainly of following types: • Long term stability. • Intermediate stability. • Accelerated stability. • In-use stability. Share this: Click to share on Facebook (Opens in new window) Facebook Click to email a link to a friend (Opens in new window)...
by maheshbhuva | Mar 9, 2023 | Method validation
Specificity As per ICH Q2A guideline defined as Specificity is the ability to assess unequivocally analyte in the present of component which may expected to present. Typically these might include impuries, degradants, matrix etc Selectivity The extent to which the...
by maheshbhuva | Feb 11, 2023 | Analytical Chemistry, GMP
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...
by maheshbhuva | Feb 6, 2023 | Analytical Chemistry, Deviation, Documents error (DIN), Pharmaceutical interview,, QMS
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...
by maheshbhuva | Jan 28, 2023 | Analytical Chemistry, Analytical method development hplc,, Hplc
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...
