what is mean by dissolution hydrodynamics?

777

---

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

904

---

what is mean by extactable and leachable study?

1105

---

how to calculate elemental impurities?

988

---

how you fix the limits of impurities?

789

---

what is mean by nitrosamine impurities?

1019

---

if instrument calibration fails then what require to do?

898

---

why require the ph, buffer during hplc mobile phase?

820

---

is it nessesary to do solution stability for 7 days?

721

---

which are the diffrent batches in the pharmaceuticals?

769

---

why xterra column require to use at higher ph?

874

---

in which situation require to take incident in validation?

1657

---

what are the guidelines for analytical method validations?

1051

---

how require to fix the linearity and accuracy cincentration range?

1577

---

how many types of balance calibration test?

2250

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