Answer Posted / mukesh tiwari

For ANDAs or US Market: One Exhibit or validation batch and
3M stability data.
For EU :Three Exhibit or validation batch and 3 M stability
data. And other supporting documents such as Pre-process
validation protocol and reports, cleaning validation, hold
time study of Bulk, Initial PQ and current one etc.

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.

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What is the basic requirement for preparing drug master file , like EDMF , USDMF ?

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what is ur strengths and weekness in ur professional life as medical rep?

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how to calculate potency of working standard by using mass balence method & this calculated potency is on as basis or on anhydrous/ dried basis

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Tell us about your oncology experience.

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How are you qualified for the position of Assistant Clinical Director?

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what is your experience in medical continuing education.

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How should the Medical Librarian interact with training staff?

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What do you mean by GTT? What are the effect of GTT on film coating.

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What are your intentions towards the uplift of the hospital.

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Caffeine standard is recommended by the monograph for HPLC wavelength accuracy calibration. It is covered range of 205 to 273 only.If the method have wavelength beyond the range, then how it supports for instrument performance?

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What experience do you have in training?

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

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pls send me last two years solved papers of health & malaria inspector to kumar.santosh087@yahoo.com

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Tell us about a situation in which you took the extra step for a patient.

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