Interested to Buy Any Domain ? << Click Here >> for more details...
Answer Posted / kishor raut
cGMP mean updating the system as per current regulation and guideline
GLP is planned, performed, monitored, recorded, reported and archived. GLP helps assure regulatory authorities that the data submitted are a true reflection of the results
obtained during the study ..
| Is This Answer Correct ? | 2 Yes | 0 No |
Post New Answer View All Answers
What r the different sop in or plant
why you are become a medical representative
Explain difference between sonication and homozinization?
how many clauses are there in iso? give me the clauses details?
from hplc chromatogram how can we say that calibration is needed now?
how to calculate potency of working standard by using mass balence method & this calculated potency is on as basis or on anhydrous/ dried basis
when i come in contact with any metal items or clothes of fur i find myself shock and when run my fingers on fur clothes or matters, i find sparks. Is there any vitiams deffecieny in my body. If so, what i have to do?
plz.mail me model papers of drug inspector of chhattisgarh..or MP.if Posible. Mail Id-recha_1428@rediffmail.com...mrs_1428@rediffmail.com,
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.
What are the filing requirements for ANDA-USA, Europe, Brazil, South Africa, Japan and Emerging Markets
What is difference between Warm and Lukewarm Water as per pharmacopia.
what is the leak test procedure of filled bottles (liquid)
please e-mail me the model of Tamil Nadu drug inspector question papers
What is the basic requirement for preparing drug master file , like EDMF , USDMF ?
