Answer / suresh naidu

Q is the specification limit( the mean of individual tablets tested should be not less than Q) of the dissolution test.

Q+5 is the criteria for which the dissolution passing with 6 tablets at S-1 stage (optimum release).:

what do you mean by mean kinetic temperature in stability

2 Answers  

---

What steps would you take to ensure responsible prescribing and prevent overuse or misuse of Alprazolam in your patients?

0 Answers  

---

What should be the LOD of dry syrup?

2 Answers   Aaheli,

---

How to measure each & every tablets hardness in compaction force control system of compression machine?

0 Answers   Macleods,

---

what is photo stability

1 Answers  

---

How to determine peak purity index in Empower software? What is the acceptance criteria of peak purity index to consider the peak purity is pass?

0 Answers   Kemwell,

---

How many types of impurites in Related compound test?

0 Answers   Aurobindo,

---

what is the exact classification of pharmaceutical industry (area wise) as per cleaning limits(Class A.B.C.D)

0 Answers   Hetero,

---

What is the difference between uniformity of content and content uniformity as official test for all tablets?

0 Answers  

---

Please send me the model papers of Drug Inspector

1 Answers   Phamatech,

---

why we use PG as a taxonomic marker ?

0 Answers   Cipla,

---

What do you mean by Q+5 in dissolution?

0 Answers  

---