Management System Certification Services

We offer a broad spectrum of certification services to assist companies to meet the necessary quality requirements and in achieving their organizational goals.

• Continuous improvement

• Error prevention

• Reduction of scattering and waste in the supply chain

• Determining and monitoring quality-related costs

• Product liability and product safety

• Determining employee and customer satisfaction

• Separate consideration of product and process development

• Interdisciplinary cooperation

ISO 9001 specifies requirements for a quality management system where an organization

• needs to demonstrate its ability to consistently provide product that meets customer and applicable statutory and regulatory requirements, and
• aims to enhance customer satisfaction through the effective application of the system, including processes for continual improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements.

ISO 14001 is an international standard related to Enviromental Management System, which specifies a set of environmental management requirements. It applies to those environmental aspects which the organization has control and over which it can be expected to have an influence.ISO 14001 can help all types of organizations to protect the environment, to prevent pollution, and to improve environmental performace. Prevention of pollution, compliance with legislation, and continual improvement are the fundamental commitments required.

IATF 16949 is a quality standard in the automotive sector which is recognised the world over, and certification to this standard is becoming an essential basis for supplying individual automotive manufacturers and international markets. A main focus of the standard is continual improvement of system and process quality in the areas of development and production. Within this context, the particular production process and its supply chain are examined so that mistakes and risks can be recognised and eliminated in order to increase customer satisfaction. As the standard is directed towards the entire manufacturing supply chain, certification to IATF 16949 can be used for both automotive manufacturers and for companies producing replacement and series production parts, and also for automotive service providers

We offer a myriad of food certification services including the FSSC/FS 22000 (Food Safety System Certification standard), the latest certification scheme for food manufacturers.

ISO 45001 is an international standard related to occupational Health and Safety Management System, which promotes a safe and healthy working environment by providing a framework that helps organizations to consistently identify and control health and safety risks, reduce the potential for accidents, aid legislative compliance, and improve overall performance. It can help organization to improve occupational health and safety performance. It applies to all types and sizes of organizations and accommodates diverse geographical, cultural, and social conditions.

ISO/IEC 27001 formally specifies a management system that is intended to bring information security under explicit management control. Being a formal specification means that it mandates specific requirements. Organizations that claim to have adopted ISO/IEC 27001 can therefore be formally audited and certified compliant with the standard.

Primarily, ISO/IEC 20000 certification demonstrates that an organization has adequate controls and procedures in place to consistently deliver a cost effective, quality IT service.

The Good Distribution Practice for Medical Devices (GDPMD) is a mandatory audit for any organizations involved with importing, wholesale and distribution of medical devices prior to their license application. Certification against GDPMD qualifies that products are consistently stored, transported and handled under suitable condition as required by the marketing authorization or product specification.

Product Conformity Assessment helps trade facilitation and protects the interests of traders: importers benefit from a faster customs clearance process because verification activities have been completed prior to shipment, and exporters do not take the risk to have their goods rejected at the country of destination because of non-compliance with the requirements.

ISO 13485 is an international standard related to Quality Management System for Medical Device. It represents the requirements for a comprehensive quality management system for the design and manufacture of medical devices. This applies not only to companies that construct, produce, and service medical devices, but also to organizations distributing and using them. ISO 13485 aims to increase the organization's reputation in the eyes of customers and authorities. ISO 13485 is not a product standard, it is a process standard which requires to comply with all relevant product and service oriented technical standards and regulations.

Aerospace organizations must produce and continue to improve safe/reliable products that meet or exceed customer or regulatory authority requirements to assure customer satisfaction. To assure customer satisfaction, suppiers to aerospace industry must produce, and continually improve, safe, reliable products that meet or exceed customer and regulatory authority requirements. The globalization of the aerospace industry, and the resulting diversity of regional/national requirements and expectations, has complicated this objective. End-product organizations face the challenge of assuring the quality of, and integrating, product purchased from suppliers throughout the world and at all levels within the supply chain. Aerospace suppliers and processors face the challenge of delivering product to multiple customers having varying quality expectations and requirements.