ISO Registration

 

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.

GET FREE CONSULTATION

    Documents Required for ISO Registration

    Letter Head

    Letter Head

    Letter Head or Visiting Card

    Registered office Proof

    Registered office Proof

    Reg.n Proof of Business

    Business

    Business

    Description of Business

    Invoice

    Invoice

    Invoice Details

    Why We Are Best

    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.

          »Single Window System

          » Save Your Time

          » Cost Efficient

          » 100% Client Satisfaction

    Our Certification Services

    ISO 9001:2015

    ISO 9001 requirements for a quality management system (QMS)

    ISO 14001:2015

    ISO 14001:2015 Requirements for an effective environmental management system ( EMS)

    OHSAS 18001:2007

    OHSAS 18001:2007 Requirements for an occupational health and safety management system

    ISO/IEC 20000-1:2018

    ISO/IEC 20000-1:2018 Requirements for the first international standard for service management

    ISO 27001:2013

    ISO 27001:2013 requirements for an information security management system (SMS) Policy & Objectives

    ISO-29990-2010

    ISO-29990-2010 Requirements for learning services for non-formal Education and Training Service Providers

    CE Marketing

    CE Marketing indicates that a product has been assessed by the manufacturer & deemed to meet EU safety

    ISO-22000/ HACCP

    ISO-22000/ HACCP Requirements for Food Safety Policy for your Organization, Developed by top management

    HACCP

    HACCP requirements for Food Safety Policy for your Organization, Developed by top management

    GMP

    GMP Quality approach to eliminate instances of contamination, mixups, and errors.

    BIFMA

    BIFMA The purpose of this document is to provide minimum requirements for claiming product conformance.

    HALAL

    Halal Certification is an official form that refers to the Halal standardization of products and/or services.

    ORGANIC

    Organic requirements for organic crops free from prohibited pesticides, herbicides and fertilizers.

    KOSHER

    Kosher requirements for a person trained and certified to butcher animals according to Jewish laws.

    RoHS

    RoHS requirements for restricts the use of specific hazardous materials found in electrical & electronic products.

    US-FDA

    US-FDA requirements for Protecting the public health by ensuring the safety in drugs, Medical devices, vaccines.

    SA 8000:2014

    SA 8000:2014 requirements for improving standards for workers and safe workplaces and health working conditions.

    IATF-16949-2016

    IATF-16949-2016 requirements for defect prevention and reduction of variation and waste in the supply chain.

    ISO-50001-2011

    ISO-50001-2011 requirements for the Develop a policy for more efficient use of energy. Fix objectives to meet the policy.

    ISO-22716:2007

    ISO-22716 requirements for the production, control, storage and shipment of cosmetic products quality and safety aspects.

    ISO-15189-2012

    ISO-15189-2012 requirements for quality and competence in medical laboratories. Used by medical laboratories in developing their QMS.

    ISO-13485-2003

    ISO-13485-2003 requirements for QMS where an firm needs to demonstrate its ability to provide medical devices and related services.

    ISO-15378-2017

    ISO-15378-2017 requirements for pharma sector to provide a QMS for suppliers of materials intended to be used as packaging.

    What are the Benefits of ISO Registration?

    The benefits of ISO Registration are mentioned below-

    What are the Benefits of ISO Registration?

    • Enhances Business Efficiency

      ISO certification plays a very essential role to build credibility in overseas business and in enhancing business efficiency.

    • Improves Marketability

      ISO Certification widens the market potential of the organization.

    • Better Customer Services

      ISO helps in improving customer services and satisfaction, to encourage the organization to deliver the best quality services.

    • Global Credibility

      If the organization wants to expand the business globally; ISO Certification plays an essential role to build credibility.

    • Improves Product Quality

      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.

    • Helpful In Government Tenders

      ISO helps the in government tenders and would give your business an advantage over your competitors.

    What is the procedure for ISO Registration?

    Registration Procedure for ISO

    • Step-1-Choosing The Kind Of Certification

      The very first step is to choose the kind of certification the organization wants.

    • Step-2-File An Application

      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.

    • Step-3-Submission Of Documents

      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.

    • Step-4-Initial Review Of The Quality Management System

      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.

    • Step-5-Preparing An Action Plan

      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.

    • Step -6-On-Premises Audit By The Registrar

      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.

    • Step-7-Obtaining ISO Certificate

      The registrar will issue the ISO certification when all the non-conformities are resolved and are updated in the ISO audit report.

    Frequently Asked Questions​

    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-

    • The company fulfills its requirement
    • Meeting customer’s requirements
    • Maintaining the proper records of documentation

    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.

    GET A FREE CONSULTATION

    Mobile : +91 - 81221 83745
    Email : support@kanakkiyal.com