Interested to Buy Any Domain ? << Click Here >> for more details...
what king of work is done in Regulatory Affairs in Pharma
industry ?
- 3 Answers
- 14923 Views
- Quintiles, I also Faced
- E-Mail Answers
Answer Posted / venkat
Regulatory affairs is a comparatively new profession which developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines
| Is This Answer Correct ? | 0 Yes | 0 No |
Post New Answer View All Answers
mode of absorption in alimentary canal?
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
How we choose the mobile phase for method development.?
what is procedure of actual procedure for registration of drug?
about method developement in hplc
What is the principle of HPLC, GC, LCMS, GCMS,LC QQQ, GC QQQ, LC Q TOF and GC Q TOF. What are the applications and Specificity?
If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
EXPLAIN THE CALCULATION PART OF AN KF TITRATOR CALIBRATION WITH SUITABLE EXAMPLE
on saturation solubility study data how we can find out the bcs class of drug?
What is gelatinization?
how to calibrate hplc & gc
what is the extinction coefficient for Indomethacin or at 319nm wave length.
which batch require to use for analytical method validation?
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?
