how you establish the LOQ?

364

---

in which situation require to use paddle and basket?

347

---

what is mean by dissolution hydrodynamics?

428

---

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

444

---

what is mean by extactable and leachable study?

646

---

how to calculate elemental impurities?

625

---

how you fix the limits of impurities?

454

---

what is mean by nitrosamine impurities?

610

---

if instrument calibration fails then what require to do?

513

---

why require the ph, buffer during hplc mobile phase?

468

---

is it nessesary to do solution stability for 7 days?

379

---

which are the diffrent batches in the pharmaceuticals?

403

---

why xterra column require to use at higher ph?

511

---

in which situation require to take incident in validation?

843

---

what are the guidelines for analytical method validations?

650

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