1.Which drugs are suitable for extended-release formulations? 2.Criteria for selection of drugs for sustained release formulation?

2 Answers   Arges Pharma Biotech,

---

Difference Between Purity And Potency?

3 Answers   Dr Reddys, Reddy Labs, Watson Pharmaceuticals,

---

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

0 Answers   Hetero,

---

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  

---

why dissolution multimedia profile of drug is important. what are the specifications for tablets ,capsules,powders etc

0 Answers  

---

why we are using toluene in resolution in UV calibration

0 Answers  

---

Why we use the placebo in analysis?

2 Answers  

---

how quantitative stability is done

0 Answers  

---

What is the difference between Drug Purity and Drug Potency?

1 Answers  

---

Why disintegration of uncoated tablets is 15 minutes why not 16 or 14 or any other value .

1 Answers   Next Wave,

---

what is photo stability

1 Answers  

---

why u want to join as a m.r?

0 Answers   Cipla, GSK,

---