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Sciences AllOther (161) [3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?
855How we can identify process related and degradation impurity in single method with short period?
870inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
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What is erythroblastosis fetalis?
can we Consider the Purity threshold and Purity angle in place of peak purity for the specificity test for method verification
what is Baculovirus Expression ?
What laboratory tests and techniques are commonly used in hematology to assess blood cell counts, morphology, and hemoglobin levels?
UV and PDA detector, which have less signal to noise ratio?
Describe a time when you worked on a team and there was a disagreement between two people. How did you handle the situation?
Can chewing on pencil is harmful for teeths?
How do you approach the use of chemotherapy and targeted therapies in cancer treatment, considering factors like tumor type, stage, and patient health?
mode of absorption in alimentary canal?
What is ultrasonic sound?
What is the difference between Discriminating media and DPDM(Dissolution Profile with Different Media)
What is the primary energy source for life on earth?
What are pericardium?
Will the plant able to produce electricity when the soil is dried up
in api coa analytical method given as Ph Europe which api used in formulation in this api coa method given Ph Europe so for Analytical methic for finished product we require to refer Ph Europe monograph ok n.a.? So any extra impurities which is given in USP monograph of api or finished product need not require to monitor on above case n.a.? but how require to do specificity?