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The ISO (International Standard Organization) certification is an important certification of the company which indicates the abilities and trust of the company and designates a company entirely meeting their customer requirements. ISO 9001 belongs to the family of ISO 9000. In the World, the ISO 9001 Standard is a widely used management system. Now you can apply for ISO certification online with us and get it easier to certify your company with ISO certification. So Let’s kick start your business with the high-end ISO certifications in India. We can help get certified with ISO 9001, ISO 50001, ISO 13845, ISO 31000, ISO/TS 16949, ISO 27000 and every other well-known certification accepted by Large scale bodies around the world. We commit our customers to certify legally and give them first priority.
ISO (International Organization for Standardization) as the name implies it’s an independent international organisation, develops International Standards, such as ISO 9001 and ISO 14001, but they are not involved in the ISO certification and do not issue ISO certificates. External certification bodies in India perform the ISO certification process.In this article we will look at ISO Certification process in detail. ISO refers to International Organization for Standardisation. It is an independent organisation that provides standards in terms of quality, safety, and efficiency of products and services provided by businesses. With the increasing competition among the business, it is important to deliver high quality of goods & services in order to sustain in the market
We have an experienced team and a huge network that will help you to get your company ISO certified. You just have to submit your basic details and we will contact you through that information and you can apply for ISO certification online. Our company is located in Delhi, so we also provide ISO certification in Delhi and all over India. We have made the process of certification easier for our customers and our customers can apply for the ISO certification online by submitting their documents online. We offer reliability and support in the process of ISO 9001 certification by updating our customers the tracking of their ISO certification.
- Step 1:
Create an application /contract – The applicant and the registrar should agree on a contract. This contract usually defines rights and obligations of both parties and includes liability issues, confidentiality, and access rights.
- Step 2:
Quality Documents Review The ISO auditor will view all your quality manuals & documents related to various policies & procedures being followed in the organization. Review of existing work will help the ISO auditor to identify the possible gaps against the requirements stipulated in the ISO standards.
- Step 3:
Make an Action Plan After the ISO auditor communicates the existing gaps in your organization, you should prepare an action plan to eliminate these gaps. Prepare the list of the required tasks to be performed to bring the desired changes in your organization. You may be required to give training to your employees to work efficiently while adapting to new procedures. Make all the employees aware of the ISO standards in terms of work efficiency and quality standards.
- Step 4:
Initial Certification Audit
- Step 5:
Completing the ISO Certification After all non-conformities are addressed and all the findings are put in the ISO audit report, the registrar will grant you the ISO certification.
- Step 6:
Surveillance Audits Surveillance audit is basically conducted to ensure that ISO quality standards are being maintained by the organization.It is conducted from time to time.
- Safety and Security
- General management
- Health and Medical
- Environment and Energy
- Information Technology
A tentative range of documents which an organization may need to exhibit their compliance during an ISO 9001:2015 audit, as categorized under Mandatory documents, Mandatory records and Non-mandatory documents, are as follows:
- Scope of the Quality Management System (QMS) (clause 4.3)
- Quality policy (clause 5.2)
- Quality objectives (clause 6.2)
- Criteria for evaluation and selection of suppliers (clause 8.4.1)
- Monitoring and measuring equipment calibration records* (clause 126.96.36.199)
- Records of training, skills, experience and qualifications (clause 7.2)
- Product/service requirements review records (clause 188.8.131.52)
- Record about design and development outputs review* (clause 8.3.2)
- Records about design and development inputs* (clause 8.3.3)
- Records of design and development controls* (clause 8.3.4)
- Records of design and development outputs *(clause 8.3.5)
- Design and development changes records* (clause 8.3.6)
- Characteristics of product to be produced and service to be provided (clause 8.5.1)
- Records about customer property (clause 8.5.3)
- Production/service provision change control records (clause 8.5.6)
- Record of conformity of product/service with acceptance criteria (clause 8.6)
- Record of nonconforming outputs (clause 8.7.2)
- Monitoring and measurement results (clause 9.1.1)
- Internal audit program (clause 9.2)
- Results of internal audits (clause 9.2)
- Results of the management review (clause 9.3)
- Results of corrective actions (clause 10.1)