Interested to Buy Any Domain ? << Click Here >> for more details...
What should be the precision for HPLC during technology
transfer?
- 3 Answers
- 9856 Views
- I also Faced
- E-Mail Answers
Answers were Sorted based on User's Feedback
Answer / glp99311
The technology transfer is nothing more than reproducing
one or more method validation parameter by second
laboratory.
The instrument precision requirement is generally the
system suitability criteria (RSD) specified in the method.
The reproducibility (precision) criteria should be the same
as performed during method validation.
| Is This Answer Correct ? | 2 Yes | 0 No |
Answer / vikram
Performing Tech. transfer activity at plant location with
System precision,Method precision,LOQ precision, specificity.
| Is This Answer Correct ? | 0 Yes | 0 No |
Answer / basha
6 times of system suitability will be considered as system
precission.6 times of different assaying is method
precission
| Is This Answer Correct ? | 2 Yes | 3 No |
What is the difference between the optics of UV and PDA Detectors ?
what is primary solution and secondary solution
For limit test of heavy metals in BP, Method C require that the substance is ignited at a temperature not exceeding 800 °C. Why confines such the temperature?
what is definition of validation? which components are followed give detail?
how require to interprit the method precision data of hptlc?
What is difference b/t uv detector and rid
what is least count of a balance? How we find out this? Any formula for least count of Analytical balance?
13 Answers Acme Formulation, Analytical Solutions, Dr Reddys, Reddy Labs,
In Number of Theoretical Plates (N) = 16 (tr/w)2. where tr: retention time, and W: peak width. My Question is here in formula what is 16.Can u explain briefly? ---Veerabhadrarao.M
3 Answers Micro Labs, Richter Themis, Sun Pharma,
Why we are use 0.005M Sulphuric acid, in control of absorbance performance test UV Spectrophotometer calibration
how many types of balance calibration test?
In dissolution test s1 stage we are getting one bowl 40 % out of 6 bowls what is the root cause you find and how proceed next step? ( Q is 80%)
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.?
Organic Chemistry 
