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 is Alcova

2 Answers   Ajanta Pharma,

---

Difference between Group-1 and Group-2 Exams

1 Answers   Asian Paints, TCS,

---

i had completed my degree with 72% but i dont have good score in gre and tofel and i got an admission into a college in usa is trheir will be any problem if i appear for visa regection because of gre and tofel and i am from science background i lost touch in those subjects.

0 Answers  

---

what is difference between uv , pda & ri detector ?

1 Answers   Strides Arcolab,

---

What is your work experience in pharmaceutical field?

0 Answers  

---

solubility of drug in penetration enhancers is affected to the transdermal penetration of any drug yes or not? increase penetration with solubility or not?

0 Answers   Zydus Cadila,

---

In resolution test of uv calibration ratio of 269nm & 266nm, respectively, using hexane as the reference . the acceptance criteria for the ratio is NLT 1.5 but always found that 1.3 ,why what i can do for the resolving the problem is it necessary to integrate exat at 269nm and 266nm ehat is limit of tollerence

1 Answers  

---

what is photo stability

1 Answers  

---

what u know about ranbaxy company

1 Answers   Ranbaxy,

---

if one drug is acidic in nature and the other drug is basic in nature, e.g. desloratadine is soluble in acidic environment i.e 0.1N HCL whereas Montelukast Sodium is soluble in basic environment i.e. .2% SLS. How can we choose a common media for there Dissolution?

0 Answers  

---

What is difference between method validation and Verification?

3 Answers   Dr Reddys, Glenmark, Larus,

---

How would you propose to advertise your drug?

0 Answers  

---