Total Quality Management is a tool to reduce the errors produced during the manufacturing or service process, increase customer satisfaction, streamline supply chain management, aim for modernization of equipment and ensure workers have the highest level of training.
Client ID: 01552 -00001
Certified by: ISO, Geneva |
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ISO 9001:2000 specifies requirements for a quality management system where an organization.
It demonstrates the ability to consistently provide product that meets customer and applicable regulatory requirements. It aims to enhance customer satisfaction through the effective application of the system, including processes for continual improvement.
Certification No: C0023856 –MDI
Certified by: ISO, Geneva |
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The primary objective of ISO 13485:2003 is to facilitate harmonized medical device regulatory requirements for quality management systems. All requirements of ISO 13485:2003 are specific to organizations providing medical devices, regardless of the type or size of the organization
Certification No: IVD/03B-09
Certified by: QSS |
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The CE marking is an assurance that the product or service so produced meets the standard internationally set for export in Europe. It is an indicator of good quality.
Certification No: GMP/193/09/2-6
Certified by: Food and Drug Administration, M.S. |
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It is the abbreviation of Good Manufacturing Practices. GMP is part of a quality system covering the manufacture and testing of active pharmaceutical ingredients, diagnostics, foods , pharmaceutical products and medical devices. GMP are the guidelines that outline the aspects of production and testing that can impact the quality of a product.