if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?

991

---

what is mean by extactable and leachable study?

1184

---

how to calculate elemental impurities?

1039

---

how you fix the limits of impurities?

841

---

what is mean by nitrosamine impurities?

1073

---

if instrument calibration fails then what require to do?

983

---

why require the ph, buffer during hplc mobile phase?

870

---

is it nessesary to do solution stability for 7 days?

786

---

which are the diffrent batches in the pharmaceuticals?

826

---

why xterra column require to use at higher ph?

924

---

in which situation require to take incident in validation?

1737

---

what are the guidelines for analytical method validations?

1110

---

how require to fix the linearity and accuracy cincentration range?

1676

---

What is difference between assay and content uniformity ?

1516

---

Human anatomy and physiology

857

---