Interested to Buy Any Domain ? << Click Here >> for more details...
IN DISSOLUTION TEST S1AND S2 AND S3 CONDITIONS ALL ARE
FAILED THEN WHAT IS THE DESSICION U CAN TAKE
- 12 Answers
- 28992 Views
- Cipla, I also Faced
- E-Mail Answers
Answer Posted / k.g.gupta dr.reddy&
Phase I investigation should be done .
As a part of Investigation,Check the previous trend data and development of the product.Root cause is not identified then raise the OOS.
Second officer results also found OOS. We can conclude that the OOS results are due to the product behavior.
| Is This Answer Correct ? | 12 Yes | 2 No |
Post New Answer View All Answers
Identify problem faced when mass spectroscopy is used with HPLC system ?
How do we get end points and how many end points are possible for citric acid and di-acid not theorotically answer should be given practically.
My question about gas chromatography sulfur chemiluminsecence detector. I test unknown sample gas by GC-SCD (calibrated ) and the result of *H2S is 279 PPM , *but when I test the same sample with the GC-TCD (calibrated ) the value of *H2S is 2500 PPM . I'd like to inform you that both GCs are calibrated and have very good operation conditions with stable parameters . the question is if the sample gas with higher H2S over detection limits of SCD detector (1000 ppm). why the result it 279 ppm Best regards
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
what is mean by 40 in the dissolution basket mesh size?
if identification threshold crosses the limits then what next step?
What is intact assay method development.....?
Why six unit used for precision?
how will you do the prep for unstable componds?
While performing TOC sst analysis Zero shift disabled & sample analysis zero shift enabled why?
In BP2013, Loperamid HCl monograph. Assay by titration with 0.1N sodium hydroxide using hydrocloric acid 0.01N and reading the volume added between the 2 points of inflexion. I have a question that if the diluent solvent is ethanol is certainly consumed a amount of volume of titrant, so this volume must be eliminated on the result calculation or not apart from first point which is subtracted above.
how to calculate elemental impurities?
what is the principle of UV Vis spectroscopy, AAS, ICP OES,ICPAES, ICP-MS and FTIR
in api coa contains only process impurities and in product coa contains degradation impurities?
In performance Check of GC Why Hexadecane Peak is ConsideredÂ
