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

340

---

what are risk assement in the analytical qbd?

283

---

why multimedia dissolution require to do?

308

---

in OSD forms require to use gas chromatography?

332

---

why require to do water content for drug product?

315

---

before starting analytical method valodation what you checking? and how giving preference to start validation?

344

---

in which situation ion pair agent require to use?

268

---

effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?

326

---

if you given one product then which tests you will perform?

319

---

on the basis of bcs class how to proceed the solubility?

279

---

for which product require to do content uniformity? what is limit of cu?

310

---

how require to select dissolution media? what is discrimination?

313

---

if rsd failed then what require to do?

320

---

if peak get problamatic then what require to do?

317

---

how you confirm the assay method?

285

---