Answer Posted / sumit palta

its not about system suitability check .its about stability program in formulated drug product by following the ich guideline Q1D.

While performing TOC sst analysis Zero shift disabled & sample analysis zero shift enabled why?

2786

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what parameters we will consider while developing a HPLC method and how we confirm our HPLC method is valid?

3630

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why we use glass fiber filters use in some situation?

734

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Difference between the quantitative analysis and qualitative analysis?

1105

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2259

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1)What's the meaning of Absorption,give a example. 2)What's the meaning of Adsorption,give a example. 2)what is the difference between Absorption and Adsorption.

2828

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What is third generation HPLC Columns?

1933

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what is mean by dissolution biowaiver study?

851

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what is the origin to prepare standard operating procedure

2248

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for heavy metal test lead used in which form pure form or any other form for preparation of lead standard sol

5990

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what is the procedure for cleaning of lenses of hatr accesory of ftir instrument?

2227

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Loss of linearity in tkn analysis, possible reasons?

1255

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how you establish the LOQ?

720

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If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?

930

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how decide the clining method and cleaning method validation require for this perticular products?

705

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