Answer / futurethoughts2000

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Answer / vanaj

the pharma qa can conduct the New implement system and
control the all departments

How do you fix the known and unknown impurity limit for a drug substance?

2 Answers   IBM,

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Which is the best Institute for Clinical Research, Clinical Data Management and Pharmacovigilance in Hyderabad?

5 Answers  

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how many persons involed for an internal audits?and who will audit the qa persons?

3 Answers   Reddy Labs,

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why use toline in resolution in uv calibration

1 Answers   Reddy Labs,

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What is the difference between Deviation and Out of Specification ?

3 Answers  

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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,

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How to register or submit drug master file to any regulatory agency?

2 Answers  

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what is your experience in medical continuing education.

0 Answers  

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Assume that you've been hired for the position. A mother calls and says her child is sick and she needs an appointment this morning. You don't have an open appointment for the morning. What will you do?

1 Answers  

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What interests you about the position of Medical Librarian in our company?

0 Answers  

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Tolerance limit for dissolution media rpm sampling point.

1 Answers   Torrent Pharma,

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How can I assign a retest date for solvents e.g. toluene, methanol, etc?

0 Answers  

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