Our Services
- ISO 9001 :2015 Certification
- ISO 14001 :2015 Certification
- ISO 45001 :2018 Certification
- ISO 22000 : 2005 Certification
- ISO 27001 :2013 Certification
- ISO 20000-1 :2011 Certification
- ISO 13485 :2016 Certification
- ISO 17100 Certification
- ISO 50001:2018 Certification
- ISO/TS 16949 : 2009
- FDA
- GMP
- HACCP
- ROHS
- CE Marking
- HALAL
ISO 9001 :2015 Certification
Overview
ISO 9001 defines the requirements for Quality Management System of an organization to Design, Manufacture and Deliver products and services to meet customer as well as applicable statutory & regulatory requirements. The standard also specifies framework to assess the customer perception and the continual improvements. ISO 9001 certification results into good management practices. The certification aims at providing a global standard that spells out quality and trust. To meet the requirements for the ISO 9001 certification, an organization should demonstrate its ability to consistently provide products that meet applicable statutory & regulatory requirements and continue to meet changing expectations of customers.
ISO 9001
The purpose of ISO 9001 is to facilitate international trade by providing a single standard that is recognized and respected globally. It is a generic standard and is applicable to organizations in all areas of work. Some of the areas are manufacturing, processing, servicing, printing, forestry, electronics, steel, computing, legal services, financial services, accounting, trucking, banking, retailing, and so on. Manufacturing, commercial and service organizations can reap many benefits from Quality Management System certification. Quality Management systems optimize production/service processes, increase efficiency and reduce costs. The ISO 9001 certificate indicates the organization’s adherence to quality management practices and minimizes the potential risk to customers. These good practices are compiled into a set of standardized requirements for a quality management system for your organization.
ISO 9001 is internationally well accepted. It is recognized in more than 160 countries and is the obvious choice for any organization involved in international business or committed to quality.
Benefits
A well designed and implemented quality management system, based on ISO 9001:2015 can provide organizations with the following benefits:
• Higher involvement and committment from top management
• Addressing risks and opportunities associated with its context and objectives
• Facilitating opportunities to enhance customer satisfaction
• Establishing framework for performance improvement
• Improves product/service reliability
• Enhanced level of employee awareness
• Better understanding of customer expectations
Highlights of ISO 9001:2015
The current version is ISO 9001:2015. This new version takes account of the increasing complexity of the environment within which organisations have to work and also focus more strongly on the special features and needs of service providers. Also a new High Level Structure will create greater harmony between ISO 9001 and other management system standards.Further, the responsibility and autonomy of organisations will be much more strongly emphasised; the same applies to the importance of the process approach and handling of risks. This standard continues to be the only non sector specific certification standard for quality management systems and maintains its most important quality objectives, such as customer satisfaction and generation of compliant products and services.
ISGS Certification services
Our team will work with your organisation to facilitate the process of achieving the certification. ISGS Certification audits certify your organisation as being committed to continual improvement and customer satisfaction. Our team of competent auditors ensures your organization’s fulfillment of customer as well as
ISO 14001 :2015 Certification
Overview
The standard defines the environmental management system requirements to which organization subscribes. The organization develops the environmental program to meet its policy, objectives and regulatory requirements and works towards continual improvement.
ISO 14001
This is the certification for companies seeking an internationally recognised environmental management system. It can help companies create a structure for managing environmental operations.
ISO 14001 specifies environmental requirements that the organisation identifies as those which it can control and influence. The standard helps organization to set the specific environmental performance criteria and improve further. The extent of the application depends on factors like the environmental policy of the organisation, the nature of its activities, products and services, the location and the conditions in which the company functions.
Highlights of ISO 14001:2015
The current version is ISO 14001:2015. This international standard is intended for use by an organization seeking to manage its environmental responsibilities in a systematic manner that contributes to environmental pillar of sustainability. It enables an organization to use common approach and risk-based thinking to integrate its environmental management system with the requirements of other management systems. This standard ensures that the environmental aspects of an organization's activities, products and services that it determines, can either control or influence considering a life cycle perspective.
Benefits of adoption
A well-defined environmental management system is essential for an organisation to manage environmental aspects like emission and handling of waste. It is important for the efficient utilisation of resources and energy. Some of the benefits of the ISO 14001 certification are:
• Enhancing environmental performance
• Life cycle perspective
• Prevention or mitigation of adverse environmental impacts
• Fulfilment of compliance obligation
• Reduction in insurance premiums; waste handling costs; water and air permitting fees
• Improved corporate image; strategic investment; improved regulatory relations
ISGS Certification services
Our team will work with your organisation to facilitate the process of achieving the certification. ISGS Certification audits certify your organisation as being committed to continual improvement and customer satisfaction. Our team of competent auditors ensures your organization’s fulfillment of customer as well as statutory & regulatory requirements.
ISO 45001 :2018 Certification
Overview
The standard defines the Occupational health & Safety management system requirements to which organization subscribes. The organization develops the program to meet its policy, objectives and regulatory requirements and works towards continual improvement of the work environment and employee health & safety.
OHSAS 45001 is a globally recognized occupational health and safety management system. The standard defines the system for an organization related to health and safety of the employees and stake holders. The standard considers Prevention as an approach towards health & safety of employees. An OHSAS 45001 certificate establishes that your organisation is committed to safety and health at the workplace. This proactive approach helps the organization to maintain the better long term relations with employees, contractors. An international standard, OHSAS 45001:2018 can integrate with ISO 9001 and ISO 14001 for environmental management systems. This is a preferred approach by management so as to take care of the risks related to product, environment and employees.
OHSAS 45001:2018 Certification
The occupational health and safety assessment series OHSAS 45001 helps organizations formulate occupational health and safety policies and objectives. The system implementation results in demonstrating the concern towards employees and safe working. The standard can be applied to Industrial as well as service sector. The extent of application of the certification will depend on factors like the occupational health and safety policy of the organisation, the nature of its activities, and the conditions under which it operates.
Benefits of adoption
• Reduction in the number of accidents and interruptions in production due to better control over hazards at the workplace
• Focus on employee safety results in a satisfied, motivated and highly productive work force
• Legal compliance with minimal administrative effort
• Improves company image and boosts international competitiveness
• Demonstrates an innovative and forward thinking approach
• Reduction in insurance costs
ISGS Certification is one of the leading certification body for auditing of certification to Integration of management systems. It is important to understand which standards can be combined and integrated. The standards which can be easily integrated are QMS, EMS, OHSAS, FSMS, EnMS, and ISMS.
ISO 22000:2005 (FSMS)
The standard defines the requirements of a food safety management system covering all entire food chain from "farm to fork", including catering and packaging companies.
Food Safety is essential requirements for a healthy nation therefore FSMS is the basic requirements of the Healthy Nation, People and for a healthy society Failures in food supply can be dangerous and cost plenty. ISO has developed the ISO 22000 standard for the certification of food safety management systems. The standard is intended to provide security by ensuring that there are no weak links in the food supply chain, and to achieve international harmonization in the field of food safety standards.
Benefits OF ISO 22000:2005 Certification
• Improvement of order efficiency of processes
• Guarantee of production process stability and high quality services
• Improvement of the firm competitive advantage
• Increase of public and state auditing bodies trust
• Increase of company price and image
• Development of the mutual confidence between a firm and a client
ISGS Certification services
Our team will work with your organisation to facilitate the process of achieving the certification. ISGS Certification audits certify your organisation as being committed to continual improvement and customer satisfaction. Our team of competent auditors ensures your organization’s fulfillment of customer as well as statutory & regulatory requirements
ISO/IEC 27001:2005/ ISO/IEC 27001:2013 ISMS
ISO/IEC 27001 is Information Security Management System. Security breaches create a risk for the enterprise. Hence, Certification to ISMS is advantageous to the organization.
Information is essential to an organization’s business and consequently needs to be suitably protected. This is essentially important in the increasingly interconnected business environment. As a result of this increasing interconnectivity, information is now exposed to a wide variety of threats and vulnerabilities. Information security is the protection of information from a wide range of threats in order to ensure :
• Business continuity
• Minimize business risk &
• Maximize return on investments and business opportunities.
Information security will function as a enabler to avoid or reduce relevant risks. Often information security management systems are challenged to demonstrate how security policies provide tangible benefits to business operations. For a effective information security management systems the approach in the organization is to align security and business goals, which enables organizational personnnel how information security adds value to business operations.
ITSM processes based on best practices of ITIL (ISO/IEC 20000-1)
ISO/IEC 20000-1 specifies requirements for the service provider to plan, establish, implement, operate, monitor, review, maintain and improve the service management system. TSM - Recognized means of benchmarking the delivery of IT to the business. Applicable to providers of IT service management services, businesses outsourcing their IT services, businesses managing their own IT services and all providers wishing to benchmark their existing IT service management services. Certification to ISO 20000-1:2011 through the scheme provides an independent, industry-wide recognition of an organization’s IT Service Management capabilities. The requirements for an organization to deliver IT services of an acceptable quality. The scope includes requirements for a management system; Planning and implementing service management; Design and transition of new or changed services; Service delivery process; Relationship processes; Resolution processes; Control processes including release and deloyment management processes.ISO 13485:2016 (MDQMS)
The objective of MDQMS i.e. ISO 13485:2016 is to facilitate harmonized and maintains medical device regulatory requirements and the requirements of the Quality management systems. Medical Equipment’s are prone to any defect which causes injury to the public health and it is very dangerous. Therefore ISO 13485:2016 certification provides and boosts a confidence and creates a credibility of the organization in the mind of the stakeholder, Directors and clients.
Benefits of ISO 13485:2016 Certification
• Increase efficiency, cut costs and monitor supply chain performance
• Increase access to more markets worldwide with certification
• Demonstrate that you produce safer and more effective medical devices
• Outline how to review and improve processes across your organization
• Meet regulatory requirements and customer expectations
ISO 17100 Certification
ISO 50001:2011 (EnMS)
Using energy efficiently helps organizations save money as well as helping to conserve resources and tackle climate change. ISO 50001 supports organizations in all sectors to use energy more efficiently, through the development of an energy management system (EnMS).
Benefits of ISO 50001:2011 Certification
• Informed decision-making processes from system design through to operation
• Increased energy awareness among staff members at all levels
• Structured approach to the Right First Time methodologies
• Improved corporate image and credibility with all stakeholders and customer
• Enhanced security of energy supply as you will have identified your energy risk exposure in areas within the organisation and commenced processes to reduce them
• Improved operational efficiencies and maintenance practices
ISO/TS 16949 : 2009
FDA
GMP CERTIFICATION
GMP defines for the goods manufacturing practices.GMP Certification is mainly developed for the natural and pharmaceutical product manufactures. It is a set of guidelines that gives you the assurance that your product is safe and correct. It is mainly dedicated for the food manufactures and medication manufactures and GMP provides assurance for produce safe and quality products according to the Quality standard. GMP is responsible for the safety, efficiency and quality of pharmaceutical products and medical devices.Benefits of GMP Certification
Application:- This is the first step to get the GMP certification, the application covers some basic information of the company. The certification body must accept the application and needs to be record or maintain all the information on the GMP database.
Review of Application:- The application received shall be reviewed by the team to ensure that the compliance requirement have been fulfilled. Quote and Agreement:- After the review of documents we provide the price quotation to the client and performs the Gap Analysis to cover all the clauses and section of the quality standards and Gap Analysis is done to check the Gap between company planned things and achieved things.
Documentation Review:- check the document of the organization to ensure that the documentation fulfilled the compliance requirement.
Stage-1 Audit:- Evaluate your organizations documented procedure and policies against the compliance requirement.
Review:- Review the documentation of your management system to ensure that the compliance requirement have been contented. Corrective action:- Corrective action is deal with the non conformity. It has taken when the non conformity occurs.
Verification:- Verify the documentation of the organization as per the standard requirements.
Stage-2 Audit:- In stage-2 audit, the auditor verifies that the organization implement according to its documentation and if the auditor of certification body identifies the non conformities then the auditor give the opportunity to correct the non conformities.
Review:- Review the implementation process according to the organizations document.
Corrective Action:- If there is any non conformity occurs then the corrective action has been taken. Verification:- Verify work instruction and implementation process are being followed by your employees.
Granting of Certification:- The Certification Body will issue a certificate of compliance, which is valid for three years.
Surveillance Audit: - Surveillance audit conduct to ensure that the organization meets the requirements of the management system. Surveillance audit must be performed in every six month or one year from the date of issued certificate.
Re-Certification:- Re-certification is the process, which is done at the end of three years period.
Review:- Review the documentation and implementation process of your management system to ensure that the compliance requirement have been contented.
Corrective Action:- Recheck the non conformity, if any other problem occurs then CB give the opportunity to the organization to resolve the non conformity.
Verification:-Compare the documentation of the organization with the compliance requirement.
HACCP
HACCP (Hazard Analysis Critical Control Point) Based Food Safety Systems
The certification is designed to prevent problems before they occur and to correct them as soon as they are detected. A process control system that identifies and prevents microbial, chemical and other hazards in food. Potential food hazards could be biological (microbes); chemical (toxin); or physical (adulterants). All the available Food Safety Systems are based on Codex Principles & HACCP Hazard Analysis Critical Control Point is a seven-step logical tool develop a food safety plan.
Identify Products of HACCP
• Identify potential food safety hazards.
• Identify critical control points.
• Establish control limits.
• Establish monitoring points.
• Establish corrective action.
• Establish effective record keeping procedures.
• Establish procedures for verification.
ROHS
ROHS refers for the Restriction of Hazards Substances. It is designed for the restriction of the use of hazardous substances in electrical and electronic equipment (EEE)". Its objective is to restrict the use of six hazardous substances within electrical and electronic equipment Such as Lead, Mercury, Cadmium, Hexavalent Chromium (Cr-VI), Polybrominated Biphenyl (PBB), Polybrominated Biphenyl ether (PBDE)
All applicable products in the EU market must pass the ROHS compliance after July 1, 2006. The mandatory requirement of ROHS directive is applicable for the European Union and the impact ofBenefits of ROHS Certification
· Mandatory requirement for the European Union. · Improve reliability and efficiency of the product. · Improve brand value and market value in the international market · It helps to the organization to produce safe products · Develops the better relationship between the client and the organizationProcess to get the ROHS Certification
· Application:- This is the first step to get the ROHS certification, the application covers some basic information of the company. The certification body must accept the application and needs to b record or maintain all the information on the ROHS database. · Review of Application:- The application received shall be reviewed by the team to ensure that the compliance requirement have been fulfilled. · Quote and Agreement:- After the review of documents we provide the price quotation to the client and performs the Gap Analysis to cover all the clauses and section of the quality standards and Gap Analysis is done to check the Gap between company planned things and achieved things. ·Documentation Review:- check the document of the organization to ensure that the documentation fulfilled the compliance requirement.
·Stage-1 Audit:- Evaluate your organizations documented procedure and policies against the compliance requirement.
Review:- Review the documentation of your management system to ensure that the compliance requirement have been contented.
Corrective action:- Corrective action is deal with the non conformity. It has taken when the non conformity occurs.
Verification:- Verify the documentation of the organization as per the standard requirements.
·Stage-2 Audit:- In stage-2 audit, the auditor verifies that the organization implement according to its documentation and if the auditor of certification body identifies the non conformities then the auditor give the opportunity to correct the non conformities.
Review:- Review the implementation process according to the organizations document.
Corrective Action:- If there is any non conformity occurs then the corrective action has been taken.
Verification:- Verify work instruction and implementation process are being followed by your employees.
·Granting of Certification:- The Certification Body will issue a certificate of compliance, which is valid for three years.
CE Marking
CE Marking is a certification mark that determines product conformity with health, safety and environmental protection standards. It majorly applies to product sold within the European economic area (EEA). Moreover, the CE marking can also be found on products that are sold outside the European economic area but are manufactured or designed in the EEA. CE Marking is also known as CE mark. CE marking certification is mandatory to export products to Euerop. With the CE marking on a product the manufacturer ensures that the product is in conformity with the essential requirements of the applicable EC directives. The letters "CE" stand for "Conformité Européenne" ("European Conformity"). Depending on the level of risk of the product, the CE Mark is affixed to a product by the manufacturer or authorized representative after ensuring that the product meets all the CE mark requirements.
Why CE Marking Is Necessary?
Getting CE marking for a product is necessary in a number of ways, some of which are listed below.
1 - CE marking on a product gives guarantees that the product is in compliance with the necessary requirements of the European health safety and environmental protection legislations. This gives credit and confidence to the manufacturers to push their products to the global market. 2-CE marking on a product also gives assurance to government officials that the product is fit enough to be placed on the market in their country, and thus enhancing global distribution of products
3-CE marking on a product also aids easy and free movement or distribution of a product within the European Union market, it also permits the withdrawal of the products that does not conform with the EEA customs and enforcement authorities or regulations.
CE Marking Process
To apply the CE marking to your product, you need to set up a technical dossier showing that your product fulfils all the EU-wide prerequisites. Being the product's manufacturer, you bear exclusive obligations for ensuring conformity with all requirements. Here are some of the processes for CE marking: Make enquiry about the EU requirements (applicable directive / rule) for your product.
Check whether your product meets the specific requirements for CE Marking.
Check whether your product needs to be tested by a Notified Body
Test your product personally & subsequently from external agency (If required for your product).
Arrange the technical dossier / technical file / technical construction file.
Affix the CE marking and draft a declaration of conformity (EU Declaration of conformity / EC Declaration of conformity.
HALAL
Halal certification is a process which ensures the features and quality of the products according to the rules established by the Islamic Council that allow the use of the mark Halal. In the case of halal food certification, every stage of food processing is examined, “from farm to table”. Halal certification tells Islamic that they can lawfully consume a company’s products based on Islamic syariah Low. This provides consumer confidence and prevents any confusion about the halal status of a product. Halal certificates are given to companies that meet the criteria and they are allowed to use a halal mark on their products. Halal product certification system also involves testing and inspection activities. The CB offering halal certification may subcontract the testing or inspection activity to another party. However, it is crucial for the CB to ensure the sub-contracted body or person is competent and complies with stipulated requirements relevant to testing, inspection or other technical activities.