why didn't you go back to previous employer after shifting to bangalore?

0 Answers  

---

What are your duties in your current position?

0 Answers  

---

please e-mail me the model of Tamil Nadu drug inspector question papers

0 Answers  

---

what is the disintegration time of mouth dissolving tablet

3 Answers   Unimarck Pharma,

---

what are the limits for LOD and LOQ? should it be necessarily less than 1?

2 Answers   Cipla,

---

What is difference between 0.1

1 Answers   Accent Pharma,

---

What is the role of Pharma QA and Validation Tester - Referring to jobs as Computer system validation analyst - interview quetions.

2 Answers  

---

while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that

0 Answers  

---

What was your most difficult experience with this population and how did you deal with it?

0 Answers  

---

Hi Sir?Mam, If i complete SAS CLINICAL in India, can i step forward to USA for job trials? How far is it possible? Am a B.pharm student ,willing to make up my Master's degree too,will this both M.Pharm and SAS help me out to get a job in USA? Please help me out with a good answer.

0 Answers  

---

How to set impurity limits for Related substances test.

1 Answers  

---

Anyone have any idea when to conduct Uniformity of Weight (UOW) and when need to conduct Uniformity of Dosage Units (UOD) or when need both? I read BP it only said if average weight < or = 0.04g then just conduct UOD, no need UOW. Under UOD section, it doesnt say when need to conduct UOD but just said UOD got two type, one is Mass Variation (MV), another is Content Uniformity (CU) and under what conditions to conduct them. For USP, no UOW section, only got UOD section.

0 Answers   Alchem, Getz Pharma Research, Hovid Berhad,

---