what do you mean by mean kinetic temperature in stability2 13247
what do you mean by bracketing and matrixing in stability1 3894
what is recovery factor1054
how much the minimum recovery should be in swab sampling1 9902
what do you mean by Q+5 in dissolution1 20299
what is difference between in drug purity and drug potency2 2736
what should be minimum limit of working standard1 14072
what is difference between method validation and method verification1 1697
what should be the LOD of dry syrup1 4866
what is relative response factor in related substance2 4143
why dissolution multimedia profile of drug is important. what are the specifications for tablets ,capsules,powders etc
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 You
at what interval Ukrainian audit will come once you register your product??
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 difference between uniformity of content and content uniformity as official test for all tablets?
What is main of k*abs in uv visible spectroscopy
what is the exact classification of pharmaceutical industry (area wise) as per cleaning limits(Class A.B.C.D)
what are the most common infectious diseases a pharmacist sees? Do pharmacists routinly encounter antibiotic resistent in some of the infectious agents that patients have contacted? if so which onces?
what is limit of cleaning validation
i am preparing for Drug inspector exam.If u have previous questions please send me.
what is difference between usfda and mhra guidline
HOW TO PERFORM SATURATION SOLUBILITY IN DISSOLUTION METHOD DEVELOPMENT?
the international interview procedure for a job.
In resolution test of uv calibration ratio of 269nm & 266nm, respectively, using hexane as the reference . the acceptance criteria for the ratio is NLT 1.5 but always found that 1.3 ,why what i can do for the resolving the problem is it necessary to integrate exat at 269nm and 266nm ehat is limit of tollerence
What is validation, validation protocol and validation master plan?