ISO 21000:2018 Management System For Educational Orgazation ISO 21001:2018 is generic and intended to be applicable to any organization that uses a curriculum to support the development of competence through teaching, learning, or research, regardless of the type, size, or method of delivery. ISO 21001:2018 can be applied to educational organizations as well as larger organizations whose core business is not education, such as professional training departments. Education is a fundamental need for everyone in society; therefore, everyone should be concerned with the quality of education delivered by educational providers. However, even though the outcomes cannot be guaranteed, educational institutions

ISO 14001:2015 Environmental System Management ISO 14001 is an international standard that focuses on the essentials for an Environment Management System. Through the more effective use of resources and reduction of waste, it improves the Environment Management System of any organization. It gives the organizations an advantage in the increasing competition and trust of Stakeholders. With the alarm of global warming and its consequence, human society has become serious about ecology and its preservation. ISO 14001 Certification – EMS helps to maintain the Environment around us, by following certain management standards. Companies adopting ISO 14001 Certification (EMS) are well placed

What Is CE Mark ? The Certificate of Conformity Europe (CE Mark) is a mark to indicate that the product to which it is affixed is in conformance with EU Product Safety Directives. These EU Directives apply to all products that are to be put into service for the first time inside the European Economic Area. The CE consultants at VAI Industrial Services know exactly what is necessary and what is not required in order to attain the Certificate of Conformity for Europe for your industrial products. Many issues arise before you can use the CE Mark, such as which

The ISO 13485 standard is for medical devices – quality management systems – requirements for regulatory purposes are the basis for regulatory compliance in local and most global markets. Exporting medical Devices to various countries is mandatory. ISO 13485 Certification is objective evidence of compliance with the requirements, regardless of the type or size of the organization. This standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and services. ISO 13485 certificate is universally