ISO 9001 requirements are general and designed to apply to all organizations, regardless of their type and size, or the products and services offered. The most approved first ISO standard on the world market.
It can be implemented in all areas of the industry and will help improve existing management processes to enable organizations to compete locally and / or globally. It helps to meet regulatory requirements and effectively implements the system to deliver real benefits to your customers.
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ISO Stands for International Standards of Organization. ISO is an independent, non-governmental international organization with a membership of 162 national standard bodies.
Certification can be a useful tool to add credibility, by demonstrating that your product or service meets the expectations of your customers. For some industries, certification is a legal or contractual requirement.
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ISO 9001 requirements for a quality management system (QMS)
ISO 14001:2015 Requirements for an effective environmental management system ( EMS)
OHSAS 18001:2007 Requirements for an occupational health and safety management system
ISO/IEC 20000-1:2018 Requirements for the first international standard for service management
ISO 27001:2013 requirements for an information security management system (SMS) Policy & Objectives
ISO-29990-2010 Requirements for learning services for non-formal Education and Training Service Providers
CE Marketing indicates that a product has been assessed by the manufacturer & deemed to meet EU safety
ISO-22000/ HACCP Requirements for Food Safety Policy for your Organization, Developed by top management
HACCP requirements for Food Safety Policy for your Organization, Developed by top management
GMP Quality approach to eliminate instances of contamination, mixups, and errors.
BIFMA The purpose of this document is to provide minimum requirements for claiming product conformance.
Halal Certification is an official form that refers to the Halal standardization of products and/or services.
Organic requirements for organic crops free from prohibited pesticides, herbicides and fertilizers.
Kosher requirements for a person trained and certified to butcher animals according to Jewish laws.
RoHS requirements for restricts the use of specific hazardous materials found in electrical & electronic products.
US-FDA requirements for Protecting the public health by ensuring the safety in drugs, Medical devices, vaccines.
SA 8000:2014 requirements for improving standards for workers and safe workplaces and health working conditions.
IATF-16949-2016 requirements for defect prevention and reduction of variation and waste in the supply chain.
ISO-50001-2011 requirements for the Develop a policy for more efficient use of energy. Fix objectives to meet the policy.
ISO-22716 requirements for the production, control, storage and shipment of cosmetic products quality and safety aspects.
ISO-15189-2012 requirements for quality and competence in medical laboratories. Used by medical laboratories in developing their QMS.
ISO-13485-2003 requirements for QMS where an firm needs to demonstrate its ability to provide medical devices and related services.
ISO-15378-2017 requirements for pharma sector to provide a QMS for suppliers of materials intended to be used as packaging.
The benefits of ISO Registration are mentioned below-
ISO certification plays a very essential role to build credibility in overseas business and in enhancing business efficiency.
ISO Certification widens the market potential of the organization.
ISO helps in improving customer services and satisfaction, to encourage the organization to deliver the best quality services.
If the organization wants to expand the business globally; ISO Certification plays an essential role to build credibility.
ISO Certification improves the product quality i.e., it should match the quality of international standard. If the standard does not match the product it will face non-acceptance on the grounds of quality issues.
ISO helps the in government tenders and would give your business an advantage over your competitors.
The very first step is to choose the kind of certification the organization wants.
Once the entrepreneur selects the ISO standard; it shall make an application in a respective form based on the ISO registrar. The application shall include the power and responsibilities of the entrepreneur and certification body.
Application shall be filed along with the requisite documents and the same shall be reviewed by the ISO certification body. ISO Certification body will review all the quality manuals and documents related to various policies being followed in the organization.
To identify any significant weakness in the Organization, the Pre-assessment (Initial review) of the Quality Management System in an organization is reviewed by the registrar and will also provide an opportunity to correct the deficiencies before the regular registration assessment is conducted.
Once the initial review of the Quality management system is reviewed, the ISO registrar notifies the existing gaps in the organization, and to eliminate these gaps the applicant has to prepare an action plan. The action plan should contain the list of the requisite work to be performed to meet the Quality Management System.
The registrar will conduct a non-premises inspection to audit the changes made in the organization. However, if the registrar finds that the requisite changes do not meet the requirements of the ISO standards, the registrar will categorize the organization into two categories depending on severity.
1. Minor Non-compliances
2. Major Non-compliances
Note-The ISO registration cannot precede until all significant non-compliances are closed by the Registrar while doing a re-audit.
The registrar will issue the ISO certification when all the non-conformities are resolved and are updated in the ISO audit report.
ISO Certification costs vary based on the size of an organization and the level to which the company is operating concerning the procedures.
No, a person cannot choose any ISO accreditation as all ISO accreditations are genuine, specific and valid. Before choosing, it is essential to pick the right ones.
Yes, one can get ISO certification for a start-up business. However, it depends on the business strategies to take up the certificate.
The ISO certificate is valid for 3 years. The re-approval or recertification can be applied before the expiry of the certificate that is before the 3rd year gets over.
ISO 9001 is described as an international standard that specifies the requirement for the quality management system (QMS). Obtaining ISO 9001 means that the organization is reflecting the following things-
ISO certification is a declaration to all the stakeholders, Shareholder of the company, Employees of the company those are working upon the prescribed rules to achieve the organization’s objectives. By obtaining the ISO certification company achieves an enhancement in credibility and customer confidence.
Yes, a person can transfer ISO certification, but for the same, the current certificate has to be accredited by an IAF or a registrar.
ISO accreditation signifies an independent 3rdparty endorsement of the certification in which the ISO certification acts as a third-party endorsement of the products/services representing the organization.
In general no, but auditors conduct surprise visits often to check if the business standards and procedures meet the required ISO mark.
ISO 27001 defines a best practice of an organization that is involved in the information security management system.
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