what is limit of cleaning validation

2504

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what is recovery factor

2227

---

how impurity is analyzed in a tablet

3456

---

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

3226

---

what is difference between temporary change control and deviation

2578

---

why we are using toluene in resolution in UV calibration

2846

---

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

3393

---

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

2918

---

how quantitative stability is done

2569

---

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

2939

---

In dissolution test why sample is withdrawn from top of the paddle and not less than 1 cm away from wall?

2498

---

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

2659

---

what is the mechanism of action of local anaesthetics?

2287

---

why we are performing linearity test for assay and rs?

2602

---

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

8921

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