Pharmacy (359)
Lab Technicians (120)
Health Pharma AllOther (113) If granules are over lubricated what defect arises in tablet compression how we solve this problem.
2161why dissolution multimedia profile of drug is important. what are the specifications for tablets ,capsules,powders etc
3065why we study matrixing in stability system in stability study and on what basis we select time point.
2220Caffeine 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?
1703
What is GLP?
what is purpose of slow,medium,fast sampling in process validation ?
plz send me previous model question paper for moh to my mail plz it's urgent my mail id is zeeta_lobo@yahoo.com
hey gyes,ve done B.SC Micro n double graduation in biochemistry, n M.Sc in MLT=PARAMEDICAL, means studied all the subjects like micro,biochem,patho,bloodbank,hematology..everything n done DISSERTATION IN CYTOGENETICS n now m looking 4 a job in banglore in some research fields..so anybody can help me to find a job..pls reply me..my email id is chaku4u@yahoo.com
You will be required to interact with patients. Tell us about your previous experience with patients and how did you deal with the experience.
What are your intentions towards the uplift of the hospital.
What are the filing requirements for ANDA-USA, Europe, Brazil, South Africa, Japan and Emerging Markets
Hai,i had completed my M.pharmacy.i want the coaching centres for drug inspector exam at hyderabad,pls help me nd wen wil b the DI exam conducted in 2012 mostly,pls also forward the model papers.. pls reply me at vislawath.jyothi@gmail.com
Do you think it is possible to rehabilitate?
how to select HPLC column for a particular product
Is there any method for calibration of HPLC ( linier gradient calibration)
why we have to use particular buffer only for dissolution instead of using cheap buffer.
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can u proceed calibration?
How to check the integrity of Sieve, Screen, FBD Bag?
what is difference between usfda and mhra guidline