Interested to Buy Any Domain ? << Click Here >> for more details...
In method developement or in any analysis if we use small
length column for analysis what happen then ? why ?
- 3 Answers
- 8075 Views
- I also Faced
- E-Mail Answers
Answer Posted / qcprashant
Resolution and theoretical plate count will also decrease
| Is This Answer Correct ? | 0 Yes | 1 No |
Post New Answer View All Answers
why require to do water content for drug product?
in each media we require to use SLS? how to proceed?
CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?
Basic principle of ESI?
what is biorelivent dissolution media?
what is different when impergnated silica plates are used in separation of azo dyes using column chromatography?
if tech transfer fails whay require to do?
How require to perform linearity as per ANVISA? What are the acceptance criteria?
what is lod and loq ?,why use k2cr2o7 , kcl h2so4 in uv calibration ?,why use benzophenone & caffene acetone in hplc calibration ?,what is leading peak in hplc ?why we do the calibration of limit of stry light in hplc & uv ?
if you get peak in blank then what require to do?
how can give the expiry period and restadardisation of volumetric solution
give clarity of linearity and range in method validation
on saturation solubility study data how we can find out the bcs class of drug?
if you have given a blank water how you analyse by general analytical techniques?
which are the diffrent batches in the pharmaceuticals?
