how you establish the LOQ?

311

---

in which situation require to use paddle and basket?

291

---

what is mean by dissolution hydrodynamics?

352

---

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

367

---

what is mean by extactable and leachable study?

565

---

how to calculate elemental impurities?

544

---

how you fix the limits of impurities?

381

---

what is mean by nitrosamine impurities?

540

---

if instrument calibration fails then what require to do?

464

---

why require the ph, buffer during hplc mobile phase?

404

---

is it nessesary to do solution stability for 7 days?

316

---

which are the diffrent batches in the pharmaceuticals?

342

---

why xterra column require to use at higher ph?

434

---

in which situation require to take incident in validation?

759

---

what are the guidelines for analytical method validations?

593

---