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JP harm Sci Bioscientific Res. 2018. 8 (1):130134ISSN NO. 22713681Review on Analytical Method for Quantitative Determination of Theophylline and in bulk and in different dosage forms 12Arina Mac wan×,
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Start by gathering all the necessary information about the analytical method that you are reviewing.
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Begin with a brief introduction to the method, including its purpose and importance in the field of analysis.
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Proceed to explain the step-by-step procedure of the analytical method, focusing on each major component and explaining the rationale behind them.
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Include any relevant equations or calculations involved in the method, ensuring they are clearly explained and justified.
05
Provide examples or case studies to illustrate the application of the method and its effectiveness in solving analytical problems.
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Evaluate the strengths and weaknesses of the method, discussing any limitations or potential sources of error.
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Summarize your overall opinion of the analytical method, highlighting its advantages and potential areas for improvement.
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Conclude the review by recommending the method's suitability for specific analytical tasks and suggesting areas for further research or development.

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Review on analytical method is needed by scientists, researchers, and analysts who aim to evaluate and compare different methods of analysis.
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It is useful for those who want to understand the strengths and limitations of a specific analytical method before implementing it in their own work.
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Industries, laboratories, and regulatory bodies also benefit from analytical method reviews as they rely on accurate and reliable analysis for quality control, product development, and compliance purposes.
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Review on analytical method is a comprehensive evaluation of an analytical method to ensure its accuracy, reliability, and validity.
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The purpose of review on analytical method is to verify the accuracy and reliability of the analytical method and ensure it meets the required standards.
The review on analytical method must include information on method validation results, instrument calibration records, and quality control data.
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