Why we are disodium tartare for factor of karlficher titration ?2 5527
any deviation can be changed into the change control?4 14469
how much newton equal to 1 kg/cm sq3 4496
What are closely monitor parameters in stability study?2 6416
what does in simple words meant by thermodynamically stable means??1 3327
hi, i am Divya from hyderabad, completed masters in pharmacy. i heard about data decoding for pharmacy professionals. so can any one give information on this like which institute offers coating for this in hyderabad and location. plz do reply.........thank you1 3253
Delay in receiving offer letter? Dear All, Recently I clear all technical and HR round with one good MNC. I've submitted my scan document of qualification and work experience. Evenafter 2 weeks of sending documents, they didn't release the offer letter. Please suggest me effective email contents to deal them. Thank You1645
why we use PG as a taxonomic marker ?
Whhat is the justification for stability study in api missed stations through deviations and statistical analysis is required.
How related substance method is developed for new compound which is not official in the pharmacopeia?
hi i have done my b pharma and now i am working as a managing director in my own manufacturing unit is there any scope overthere 4 me
What is validation, validation protocol and validation master plan?
How we fix the validity period of a volumetric solution and re-standardization due date?
What is the difference of vacuum pressure and vapor pressure?
What is the relative response factor in related substances?
what is the difference of vaccum pressure and vapour pressure ?
when we calibrate uv for control of wavelength we scan for 200 to 800 nm but we get the result only for some specific wavelength how we confirm for all other wavelength?
what is the calculation for getting the tablet weight and the punch size, Eg..if there is a 8/32 punch then how to measure tablet weight????
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 email@example.com
Why and When RRF is necessary in RS method? How it is helpful in method development?
what is the exact classification of pharmaceutical industry (area wise) as per cleaning limits(Class A.B.C.D)
Why should we not dispatch the reprocess material to export?