which are the sizes of capsules?

398

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if content uniformity passing but dissolution varrying then what is next step?

380

---

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

332

---

what are risk assement in the analytical qbd?

278

---

why multimedia dissolution require to do?

303

---

in OSD forms require to use gas chromatography?

326

---

why require to do water content for drug product?

311

---

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

334

---

in which situation ion pair agent require to use?

265

---

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

320

---

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

312

---

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

273

---

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

304

---

how require to select dissolution media? what is discrimination?

306

---

if rsd failed then what require to do?

313

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