what is limit of cleaning validation

2453

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what is recovery factor

2171

---

how impurity is analyzed in a tablet

3351

---

how you can fix the known and unknown impurity limit for any drug substance

3166

---

what is difference between temporary change control and deviation

2457

---

why we are using toluene in resolution in UV calibration

2769

---

what is difference between uniformity of content and content uniformity as official test for tablet

3332

---

if calibration of 12 bowl dissolution apparatus does not meet a single stage procedure how you can proceed calibration

2869

---

how quantitative stability is done

2503

---

what is purpose of slow,medium,fast sampling in process validation ?

2874

---

In dissolution test why sample is withdrawn from top of the paddle and not less than 1 cm away from wall?

2438

---

In HPLC- wavelength calibration calculation why we are taking peak height and why should not take peak area?

2608

---

what is the mechanism of action of local anaesthetics?

2225

---

why we are performing linearity test for assay and rs?

2554

---

why some samples are taking 500mg for water content and some samples are taken 2g for water content?

8832

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