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Focus Certification was established in 2010. with wide presence in India & 12 locations abroad and employing more than 80 full-time personnel, Focus is never very far from its Clients. It is easily recognized by all stakeholders as one of the most competent, ethical & professional service. Being the market leader, We offer very comprehensive and diverse range of technical services to our clients. Our Clientele includes some of the Leading corporate houses, Public sector organizations, medium and small scale enterprises. Focus Certification Limited. provides diverse services in Management Systems - Quality, Environment, Safety, Food, Information Technology, and Social accountability. Training in allied areas like Lead Auditor, Internal Auditor & awareness courses.
Third Party Inspection,Product Certification (CE), Automotive Homologation, Six Sigma etc. Focus is Accredited with Global UK, with Accreditatin for Management System Certifications i.e. ISO 9001:2015, ISO 14001:2015, OHSAS 18001:2007, ISO 45001:2018, ISO 20000-1:2011, ISO 27001:2013, ISO 22000:2005, ISO 22000:2018, ISO 50001:2011 and ISO 13485:2016 and FSSC 22000, ISO 39001:2012, ISO 21898:2004, ISO/IEC 27018:2014, ISO 10668:2010, ISO 21001:2018, ISO 10004:2018, ISO 10002:2018, ISO 20121:2012, ISO 22301:2012, Iso 37001:2016, ISO 55001:2014, ISO 29990:2010, ISO 41001:2018, ISO 20000-1:2018.
MANAGEMENT SYSTEM CERTIFICATIONS
We enable you to demonstrate your business, Products, Process and system which is compatible with the national or international guidelines or customer defined standards through certifications.
The world cannot sustain without the support of one another. We are associated with various international certification bodies who provide various Product certifications like CE mark, ISI mark, Rohs, FCC and many more…
We provide the training as per the standards and guidelines developed for the proper management of the system , organization , process in compliance with the national or international standards such as ISO 9001, ISO 14001, OH&S 18001, ISO 22000, ISO 27001 and various other standards.
We are associated with various international certification bodies who provide certifications which are as per the religious guidelines of various religious community. These certifications are namely KOSHER, HALAL, etc.
Why Choose Focus?
We have been serving from few decades and today we have become one of the leading certification body for management system standards like ISO 9001, ISO 14001, OH&S 18001, ISO 22000 and various other standards. We help over 10,000 organizations ranging from top global brands to small business enterprises in more than 25 countries worldwide. As one of the few organizations that understand the standards from start to finish, we don’t only access how well you are meeting the requirements of the standard but we give you the required improvements which can transform your organization.
We at Focus are highly organized, great at collaboration, accountable, Committed, we follow FFF (Find, Fix and Finish) the problem solving approach, Equally aligned to all the customers and we also respect punctuality. And here come the exact answer why we.yes because you will exactly what you want and we are here only for you we are highly customer oriented.
1. ISO 9001 is defined as the international standard that specifies requirements for a quality management system (QMS). Organizations use the standard to demonstrate the ability to consistently provide products and services that meet customer and regulatory requirements.
2. ISO 14001 is the international standard that specifies requirements for an effective environmental management system (EMS). It provides a framework that an organization can follow, rather than establishing environmental performance requirements.
3. OHSAS 18001, Occupational Health and Safety Assessment Series,is a British Standard for occupational health and safety management systems. Compliance with it enables organizations to demonstrate that they have a system in place for occupational health and safety
4. ISO 27001 is a specification for an information security management system (ISMS). An ISMS is a framework of policies and procedures that includes all legal, physical and technical controls involved in an organisation’s information risk management processes.
5. ISO 45001 is an International Standard that specifies requirements for an occupational health and safety (OH&S) management system, with guidance for its use, to enable an organisation to proactively improve its OH&S performance in preventing injury and ill-health.
6. ISO 22000 is a Food Safety Management System that can be applied to any organization in the food chain, farm to fork. Becoming certified to ISO 22000 allows a company to show their customers that they have a food safety management system in place. This provides customer confidence in the product.
7. ISO 50001 Energy management systems– Requirements with guidance for use is a specification created by the International Organization for Standardization (ISO) for an energy management system.
8. IATF 16949:2016 (replaces ISO/TS 16949:2009) is a standard that establishes the requirements for a Quality Management System (QMS), specifically for the automotive sector. Failure to conduct the audit within the allowable timing requirements requires the organization to start over with an initial certification audit
Wish to Go for ISO Certification?
Fill the below form to apply for ISO Certification such as ISO 9001 Certification, ISO 14001 Certification, ISO 45001 Certification, ISO 22001 Certification, OHSAS 18001 Certification, ISO 27001 Certification and various other certification.
Focus CB audit process is a comprehensive and objective audit of the management system to which an organization operates. The initial assessment is conducted in two stages, followed by the certification, surveillance, and recertification processes which are described below:
STAGE 1 AUDIT
The Stage 1 Audit is conducted virtually or on-site at the client’s facility.
The objectives of this audit are as follows:
Audit the management system documentation
Evaluate the location(s), site-specific conditions and undertake discussions with personnel
Collect information related to the scope of the management system and related statutory and regulatory requirements
Confirm management reviews and internal audits are being planned and performed
Determine preparedness for the Stage 2 Audit
Produce a process-based audit plan for the Stage 2 Audit visit
The period between Stage 1 and Stage 2 audit is normally 30 days.
STAGE 2 AUDIT
The Stage 2 audit is conducted on-site at the client’s facility to evaluate the effectiveness of management system implementation.
The objectives of this audit are as follows:
Gather information and objective evidence regarding the applicable standard being audited
Verify performance monitoring, measuring, reporting and reviewing key performance objectives and targets
Verify management system performance regarding legal compliance
Determine operational control of the management system processes Verify internal audits and management reviews have been planned and performed
Review management’s responsibility for policies
Confirm links between policy and legal requirements as well as procedures and data .Determine the competence of personnel
Annual Surveillance Audits
After issuance of the certificate of registration, surveillance audits must be conducted at least once a year.
The date of the first surveillance audit following initial certification shall not be more than 12 months from the last day of the Stage 2 Audit to ensure the certification remains valid and does not expire
A re-certification audit is planned and conducted at client’s facility 36 months after the initial certification to evaluate continued fulfillment of all of the requirements of the relevant management system standard as well as the continued improvement of the management system
CB audit team works with clients to keep track of and schedule the date of their next required audit. It is our promise to conduct a comprehensive audit of a client’s management system while remaining impartial throughout the certification cycle. The competence of our auditors and effectiveness of our audit processes will enable clients to gain full value of an implemented management system.
Nonconformity is a non-fulfillment of a requirement and can be found during an audit. Nonconformities can be classified in two ways: major and minor. A major nonconformity affects the capability of the management system to achieve the intended results. If there is a significant doubt that effective process control is in place, or that products or services will meet specified requirements a nonconformity can be found. Additionally, a number of minor nonconformities associated with the same requirement or issue could demonstrate a systemic failure and thus constitute a major nonconformity. A minor nonconformity does not affect the capability of the management system to achieve the intended results.
If a nonconformance is found during an audit, the auditor will identify in detail the objective evidence on which the nonconformity is based and discuss with the client to ensure that the evidence is accurate and the nonconformities are understood without suggesting a cause of nonconformities or their solution.
CB requires the client to analyze the cause of and describe the specific correction and corrective actions taken or planned to be taken, to eliminate detected nonconformities, within 30 days.
This process and the requirements are described in more detail as required, during an audit.
ISO 45001- Occupational health and Safety Management System Lead Auditor Training
The most awaited Standard ISO 45001- Occupational health and Safety Management System is now published.
ISO 45001 is intended to replace the most widely implemented international standard BS OHSAS 18001 which will be replaced by ISO 45001 within 3 years of release of ISO 45001 international Standard.
Management system training programmes are conducted with an aim to develop a healthy culture of implementation of the ISO standards in industries. The ISO Training helps the organization to understand the basic requirements of the standard, ISO Training helps organization how to implement the ISO standard and creates an interest to the people involved in the ISO Standard Implementation. ISO Training helps to create the core team for the implementation of the ISO standard. ISO Training helps to create a team for the internal audits which adds a value to the organizational process.
In addition to that there are Lead Auditor courses which helps the individuals to become competent auditors for auditing management systems with respect to the Quality- ISO 9001, Environmental Management system- ISO 14001, Occupational health and safety- OHSAS 18001/ ISO 45001, Food Safety Management system- ISO 22000, HACCP, Energy Management system- ISO 50001, Information Security Management system- ISO 27001, Quality System for Medical Devices Manufacturing- ISO 13485, Anti Bribery management system- ISO 37001 and many more ISO Standards.
Awareness and internal auditor Training for ISO 9001, ISO 14001, ISO 22000, ISO 45001, ISO 22000, ISO 27001, ISO 13485, ISO 50001, ISO 37001, IATF 16949 and various other management system standards.
The innovative workspace
Professional and timely service delivery of service
We are certificates from focus since 2014 , Good services
Auditor are good and professional
Good training services , expert trainer
WE PROVIDE SERVICES FOR:
Inspection and Testing
In commercial transactions, many organizations employ the services of inspection agents to ensure the shipment quantity and product quality is in conformity with contractual requirements. The professional inspection operations of GR offer strong logistic support to clients when quality issues. All inspections can be carried out to ISO 17020 Requirements.
Initial Production Checks
GR inspects the quality of materials, parts and components at the initial stage of production to ascertain conformity with specified requirements. Production samples will be drawn randomly and checked to assure they meet specifications. Valuable data will be generated for continuous improvement in the production process.
In Process Inspections
GR steps in again when the production reaches approximately 30% of the quantity manufactured. The objective of this is to ensure that any quality problems previously identified are completely rectified and that the product quality conforms to client requirements.
Final Random Inspection
Upon completion of the production, GR inspects against specifications and defect classification. All findings are reported to clients promptly by fax or email before the issuance of the final report.
We are able to carry out inspections of your facilities, equipment and products, and audits of your systems and processes against practically any referential, on a local or worldwide basis. In a number of cases, inspections and audits will ultimately enable us Grant a certification to your organization
GR has a unique approach of certification which complies with the requirement for bodies providing Inspection and certification.
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