Quality Control of Analytical Methods
Quality control, or QC for short, is a procedure by which elements audit the quality of all elements engaged with creation. ISO 9000 characterizes quality control as "A piece of quality administration concentrated on satisfying quality necessities". Components, for example, controls, work administration, characterized and all around oversaw procedures, execution and respectability criteria, and recognizable proof of records Competence, for example, knowledge, skills, experience, and capabilities. Delicate components, such as personnel, integrity, confidence, organizational culture, motivation, team spirit, and quality relationships. Controls incorporate item assessment, where each item is inspected outwardly, and frequently utilizing a stereo magnifying instrument for fine detail before the item is sold into the outside market. Examiners will be furnished with records and depictions of unsuitable item deformities, for example, breaks or surface flaws for instance. The quality of the yields is in danger if any of these three angles is insufficient in any capacity.
- Control of errors in analysis
- Accuracy & Precision
- Validation of analytical procedures
- Compound random errors
- Basic calculations in pharmaceutical analysis
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Quality Control of Analytical Methods 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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