Good Manufacturing Practices (GMP, also referred to as 'cGMP' or 'current Good Manufacturing Practice') is the aspect of quality assurance that ensures that medicinal products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the product specification.
In conclusion, adherence to CGMP regulations is crucial for ensuring the safety, efficacy, and quality of pharmaceutical products. Failure to comply with these regulations can result in serious consequences for both patients and the pharmaceutical industry. Some common CGMP violations that must be avoided include inadequate cleaning and sanitation, improper documentation and record-keeping, lack of proper validation and testing, and failure to follow proper procedures for handling and storing materials. By prioritizing CGMP compliance and implementing effective quality management systems, pharmaceutical companies can maintain their reputation and ensure the safety and satisfaction of their customers.
Six sigma concepts in quality management systems |
Pharmaceuticals industry, GMP violations, How to Avoid GMP Errors,
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industrial Pharmacy | Pharm-D.
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