how decide the clining method and cleaning method validation require for this perticular products?

308

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How to set analyticl specification for combination products?

306

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How doing qbd practically?

434

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which situation gc hs and gc als require to use?

301

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on saturation solubility study data how we can find out the bcs class of drug?

368

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identification is for unknown? qualification for known? reporting for LOQ?

289

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Which parameter require to do for analytical method equivalency?

326

---

what is biorelivent dissolution media?

308

---

in which situation require to change rs specification?

278

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If combination product how require to identify which imp is of which api?

327

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in which situation ion pair require to use?

281

---

What is shaking level in GC?

334

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What is split ratio in Gc? Splitless? how requirr to select?

328

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why digestion require in icpms?

309

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[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?

357

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