What is mean by PDR?

949

---

What is the accrptance criteria in RSD for RS method precision on basis of impurity percentages?

830

---

Related substance method equivalency on control sample or spiked sample?

771

---

How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?

735

---

how to develop the icp ms method? Application of icp ms?

812

---

What is the diffrence in japan mkt requirement in analytical method validation over US?

725

---

From where require to take the RLD sample?

759

---

if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?

684

---

in dissolution if one bowl got 70 percent 2nd bowl got 80 percent and 3rd bowl got 90 percent then how proceed?

759

---

if you have given one product then how you determine the impurity in that?

744

---

Is it nessesary all multimedia dissolution require descriminatory?

800

---

which are the sizes of capsules?

972

---

if content uniformity passing but dissolution varrying then what is next step?

883

---

what is classification of elemental impurities? what is risk assement in elemental impurities?

760

---

what are risk assement in the analytical qbd?

764

---