The ISO 9000 family of standards is a guideline on good quality management practices. This standard consists of standards and guidelines relating to quality management systems and related supporting standards...
ISO 14001: 2004 specifies requirements for Environmental Management System (EMS) for any organization that seeks to demonstrate compliance with laws and regulations, and conformity to environmental policy and...
OHSAS ISO 18001:2007 Occupational Health & Safety Assurance System (OHSAS) is a prevention based safety system designed to safe guard the safety and health of employees of the Company. OHSAS...
Using this family of standards will help your organization manage the security of assets such as financial information, intellectual property, employee details or information entrusted to you by third parties...
ISO 50001:2011 identifies needs for establishing, implementing, maintaining and improving an energy management system, whose purpose is to allow an organization to follow a systematic,ISO 50001:2011 identifies needs ...
ISO 13485, Medical devices – Quality management systems – Needs for regulatory purposes, is a globally agreed standard that sets out the needs for a quality management system exact to the medical...
The ISO 9000 family of standards is a guideline on good quality management practices. This standard consists of standards and guidelines relating to quality management systems and related supporting standards.
ISO 14001: 2004 specifies requirements for Environmental Management System (EMS) for any organization that seeks to demonstrate compliance with laws and regulations, and conformity to environmental policy and stated...
ISO 22000/HACCP is developed by ISO to deal with the food safety. With the increasing demand of the processed food, and other eatable products, there was a need for an internationally recognized standard that takes care ....
OHSAS ISO 18001:2007 Occupational Health & Safety Assurance System (OHSAS) is a prevention based safety system designed to safe guard the safety and health of employees of the Company.
ISO 45001:2018 identifies needs for establishing, implementing, maintaining and improving an Occupational Health and Safety Management System with the overall purpose remaining the ...
A GMP is a system for confirming that products are constantly produced and controlled according to quality standards. It is designed to decrease the risks involved in any pharmaceutical...
ISO 13485, Medical devices – Quality management systems – Needs for regulatory purposes, is a globally agreed standard that sets out the needs for a quality management system exact to the medical devices industry. It has lately been revised, with the new version published in March 2016.
There is no single reason that would necessitate you getting ISO certified. It may be a requirement of your buyer, rules for the country where you plan to export, some government tender requirement or simply a management decision to help improve business credibility and authority as well as the overall efficiency of the business.
Certification cost is determined by a lot of factors including the type of certificate, number of certifications applied, size and business of the entity. So to have an estimate of the pricing we recommend you to reach out to our team for further details on verify@glscert.org . with your entity details.
ISO certification is not a single event, but rather an ongoing process that ensures your business complies with the requirements of its chosen standard. Initial certification depends on how many ISO standards you are trying to achieve and the setup of your organisation. Following certification, there is a process for continual improvement and recertification. Find out more about the process at glscert.org ..
There are more than 20,000 types of certifications! Hence, we recommend getting in touch with our experts at verify@glscert.org with your requirement and we shall suggest the most appropriate certifications beneficial for your business