Interested to Buy Any Domain ? << Click Here >> for more details...
Tolerance limit for dissolution media rpm sampling point.
- 1 Answers
- 3945 Views
- Torrent Pharma, I also Faced
- E-Mail Answers
Answer Posted / ankalreddymsc
RPM : +/- 1
Dissolution medium : 10% of measured volume
Sampling time : +/- 30 seconds from time point
| Is This Answer Correct ? | 0 Yes | 0 No |
Post New Answer View All Answers
How can I assign a retest date for solvents e.g. toluene, methanol, etc?
Tell us about your oncology experience.
What is forced degradation study?
Do you think it is possible to rehabilitate?
what is your experience in medical continuing education.
What skills have you acquired that would apply to the position of Clinical Data Manager?
Hi Sir?Mam, If i complete SAS CLINICAL in India, can i step forward to USA for job trials? How far is it possible? Am a B.pharm student ,willing to make up my Master's degree too,will this both M.Pharm and SAS help me out to get a job in USA? Please help me out with a good answer.
Tell us about a time when you failed to meet a deadline. What were the repercussions?
Caffeine standard is recommended by the monograph for HPLC wavelength accuracy calibration. It is covered range of 205 to 273 only.If the method have wavelength beyond the range, then how it supports for instrument performance?
How should the Medical Librarian interact with training staff?
Can any one tell me that which brand hplc column is used for levetiracetam imp- b test.
Anyone have any idea when to conduct Uniformity of Weight (UOW) and when need to conduct Uniformity of Dosage Units (UOD) or when need both? I read BP it only said if average weight < or = 0.04g then just conduct UOD, no need UOW. Under UOD section, it doesnt say when need to conduct UOD but just said UOD got two type, one is Mass Variation (MV), another is Content Uniformity (CU) and under what conditions to conduct them. For USP, no UOW section, only got UOD section.
how to calculate potency of working standard by using mass balence method & this calculated potency is on as basis or on anhydrous/ dried basis
from hplc chromatogram how can we say that calibration is needed now?
why nitrogen charecter as a inert gas plz identified
