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TOTAL QUALITY MANAGEMENT, QUALITY REVIEW AND DOCUMENTATION
  • Pharmaceutical Analysis

5. TOTAL QUALITY MANAGEMENT, QUALITY REVIEW AND DOCUMENTATION

Total Quality Management (TQM) refers to management methods used to enhance quality, based on the participation of all members & aiming all long term success through customer’s satisfaction & benefits…

GLP, ISO 9000
  • Pharmaceutical Analysis

4. GLP (Good Laboratory Practice), ISO (The International Organization of Standardization ) 9000

Good Laboratory Practice is defined in the OECD Principles as “a quality system concerned with the organizational process and the conditions under which non-clinical health and environmental safety studies are…

VALIDATION METHODS - QUALITY OF EQUIPMENT, VALIDATION OF EQUIPMENT AND VALIDATION OF ANALYTICAL INSTRUMENTS AND CALIBRATION
  • Pharmaceutical Analysis

3. VALIDATION METHODS – QUALITY OF EQUIPMENT, VALIDATION OF EQUIPMENT AND VALIDATION OF ANALYTICAL INSTRUMENTS AND CALIBRATION

VALIDATION: The validation of a test method is the process by which the relevance and reliability of the method are assessed for a particular purpose. CALIBRATION: Calibration is the activity…

CONCEPT OF STATISTICAL QUALITY CONTROL
  • Pharmaceutical Analysis

2. CONCEPT OF STATISTICAL QUALITY CONTROL

Statistical quality control must be regarded as a package of gear which can also additionally have an impact on selections to the features of specification, manufacturing or inspection. CHARACTERISTICS OF…

INTRODUCTION, SOURCES OF QUALITY VARIATION, CONTROL OF QUALITY VARIATION
  • Pharmaceutical Analysis

1. INTRODUCTION, SOURCES OF QUALITY VARIATION, CONTROL OF QUALITY VARIATION

Quality Variation: When the first-rate of any drug is given via way of means of industry, then it’s far accountable for any variant from the standard. Quality Variation might also…

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