Analytical Methods and Control Strategies
Of late there is a marked interest in enhancing the approaches for analytical method development, validation, and lifecycle management. Most of these are aligned to Quality by Design (QbD) approach for drug development. The enhanced approaches mostly utilize risk assessments and in-depth systematic evaluations of critical method variables to identify the controls required to ensure that the measurement uncertainty of a reportable result is controlled to a level that ensures that the method is “fit for purpose”. Traditional subjective methods use partitions, for example, precipitation, extraction, and distillation. ID might be founded on contrasts in color, odor, melting point, boiling point, radioactivity or reactivity. Established quantitative analysis uses mass or volume changes to measure sum.
- Physical Analytical Methods
- Titrimetric Methods
- Specific methods
- Reagents
- Miscellaneous Methods
Related Conference of Analytical Methods and Control Strategies
November 25-26, 2025
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Analytical Methods and Control Strategies Conference Speakers
Recommended Sessions
- Analysis of Pharmaceutical Agents
- Analytical Method Development and Validation
- Analytical Methods and Control Strategies
- Biopharmaceutical Research & Development Process
- Chromatography & Separation Techniques
- Drug Discovery & Development
- Electroanalytical Methods
- Errors in pharmaceutical analysis & statistical validation
- GLP and GMP Method Development, Validation and Remediation
- Modern Pharmaceutical Analysis
- Pharmaceutical and Biomedical Analysis
- Pharmaceutical Microbiology
- Pharmaceutical Nanotechnology
- Preformulation Studies
- Quality Control of Analytical Methods
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