Quality Management System
Quality Management Standard
A process that prevents defects & losses by implementing better planning, applying industry proven practices at every step of business cycle is called "Quality Management System".
Performance Criteria for Authentication Solutions
In order to combat with piracy and counterfeiting of material goods, ISO 12931 - Performance Criteria for Authentication Solutions Standard (PCAS) is used.
Six Sigma Methodology
Six Sigma Methodology or DMAIC Methodology can help existing business processes and procedures by utilizing its core mechanism which consists: Define, Measure, Analyze, Improve and Control.
Medical Laboratories Accreditation Program
CAP stands for The College of American Pathologists, the largest association of pathologists. American Board of Pathology (ABP) certifies and monitors CAP. For laboratory quality assurance, CAP is accepted as a global leader.
Medical Devices Quality Management System
ISO 13485 emphasizes on medical devices manufacturing industry's regulatory requirements. Medical Devices Quality Management System Standard focuses on risk factors and monitors the overall product development process.
Medical Laboratory Accreditation
ISO 15189 pint points the requirements for competency assessment and quality assurance in medical laboratories. Medical laboratories use this accreditation to develop their quality management system and for accessing their competence.
Inspection Bodies Accreditation
Proper implementation of ISO 17020 is very important for overall maintenance of machinery, plant, tools, infrastructure, processes and system itself. Inspection Bodies Accreditation, monitors technical competence of quality management system and provides guidelines to achieve consistent and accurate inspection processes.
Personnel Certification Bodies Accreditation
ISO/IEC 17024:2012 : Conformity Assessment is also known as general requirements for Personnel Certification Bodies Accreditation. It sets a unanimous benchmark for certification programs to ensure that certification process remains consistent, relatively comparable and reliable globally.
ISO/IEC 17025 Laboratory Accreditation Standard is for improving overall quality of a Laboratory. ISO 17025 fulfills the requirements of highly technical competence and management system thus ensuring your test results & calibrations are consistently accurate.
Accreditation of Reference Material Producers
In the process of validation, process measurement, quality control and calibration, Reference Materials (RMs) are used. Regulatory authorities and accreditation bodies also use ISO/IEC 17034:2016 - Accreditation of Reference Material Producers for the assessment of competency.
Good Laboratory Practice (GLP)
A set of principles used to ensure the quality, consistency, accuracy and integrity of a non clinical laboratories is called Good Laboratory Practices or GLP. These non clinical laboratories do the research and marketing work for the products regulated by the government.
Product Certification Bodies Accreditation
ISO 17065 (ISO/IEC 17065) is a Product Certification Bodies Accreditation Standard. As the name says it loud and clear, this standard is for the bodies who are certifying the quality of a product.
Management System for Records
ISO 30301 helps organizations to implement Management System for Records (MSR). Organizations can achieve business efficiency with the help of MSR. This standard also makes organizations accountable for their services, increases continuity & consistency and also helps to manage risks.
ISO 21500 is derived from ISO 10006 and provides guide lines for Project Management and is more comprehensive as compared to ISO 10006. ISO/IEC 21500 specifies concepts and processes that are needed for improving performance of projects.