Answer / lingareddy

while entrer into the plant we give training on cgmp ,
plant hygiene policy, safety then common sops related to
QA , engineering Then related department sops

Answer / rakesh desai(sun pharma)

First introduce the company policy about quality,safety and
decipline reqirment,Followed by induction and quality
system.Then followed by department system and department
practical training.During each stage evolution required to
forward him/her for the next stage training.

Answer / yogesh shinde

FIRST WE WILL CHECK THE BASIC KNOWLEDGE IN CHEMISTRY
[ANALYTICAL OR ORGANIC CHEMISTRY]
ACCORDING TO THAT WE WILL TRAIN HIM

What is (Q) point dissolution?

6 Answers   Cipla, Macleods,

---

Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?

0 Answers   IDA,

---

What is FDA form 482c?

1 Answers   Lupin,

---

how can we determine RRF value in HPLC FOR CALCULATION OF IMPURITY ?

4 Answers   Macleods,

---

for which type of applications gas chromatography is used?

2 Answers  

---

what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.

0 Answers  

---

what type of compounds do we see lod @ wat type compounds do we see m.c

3 Answers   Orchid,

---

what is the difference between potentiometric assay and hplc assay

2 Answers   Parabolic,

---

Why we perform the ir analysis?

3 Answers   Sequent,

---

In gas chromatographic analysis sometimes we use headspace, why it is required instead of manually injection?

1 Answers  

---

Difference Between End Cap HPLC Column and Non End Cap Column

2 Answers  

---

How we can identify process related and degradation impurity in single method with short period?

0 Answers  

---