DGA CERTIFICATION

About DGA CertificationDGA Certification is an ISO certified organization provides customization consulting, training, auditing and certification services that reduces risks and save time for organizations while educating, empowering and enabling leadership to implement, improve and integrate management systems and strategic initiatives.

DGA Certification is the leading, fast growing, professional and cost effective ISO certification service in India. It performs initial registrations and periodic surveillance reviews to assure that your quality, environmental, or sector-specific system is being maintained in accord with the ISO standards. It is global proof that your company has met and continues to meet all the requirements of the ISO standard that your business is seeking.

Customer satisfaction, credibility, integrity of the staff and value-added services are the key benchmarks that determine the total value of the relationship. By selecting DGA Certification as your partner for management system certification, you are selecting the company that makes a serious commitment to all its clients.

ISO 9001:2015 Certification (QMS)

ISO 9001 is 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. It is the most popular standard in the ISO 9000 series and the only standard in the series to which organizations can certify.

ISO 9001 was first published in 1987 by the International Organization for Standardization (ISO), an international agency composed of the national standards bodies of more than 160 countries. The current version of ISO 9001:2015 was released in September 2015.

ISO standards are reviewed every five years by the standards committee responsible for their relevance, suitability and effectiveness. At the recent review, a majority of the ISO committee decided that ISO 9001, the current standard for quality management, needed revising. The new version is now published and replaces the 2008 version. The associated changes and impacts will make the ISO 9001 quality management system relevant for companies all

DGA CERTIFICATIONaround the world regardless of their size or industry. On this page, we have gathered together the most important information on the new version of the quality management standard ISO 9001.

Benefits of iso 9001 certification (qms)v Improve your market access opportunities and gain a competitive advantage.

v Increase the efficiency within your organization.

v Reduce errors and complaints.

v Generate trust with your customers.

v Increase the customer orientation of your business.

v Achieve significant cost savings.

v Improve your processes and structures sustainably.

v Motivate their employees through better communication and readily available information.

ISO 14001:2015 CERTIFICATION (EMS)

ISO 14001:2015 specifies the requirements for an environmental management system that an organization can use to enhance its environmental performance. ISO 14001:2015 is intended for use by an organization seeking to manage its environmental responsibilities in a systematic manner that contributes to the environmental pillar of sustainability.

ISO 14001:2015 helps an organization achieve the intended outcomes of its environmental management system, which provide value for the environment, the organization itself and interested parties. Consistent with the organization's environmental policy, the intended outcomes of an environmental management system include.

An environmental management system certified by DGA CERTFICATION in accordance with ISO 14001 is not just globally valid and recognized throughout the world. It also opens to you the forward-looking path towards personal

DGA CERTIFICATIONresponsibility and commitment. It is now a matter of course for most companies to seek improvement in their performance in protecting the environment and to provide evidence of this.

With an environmental management system certified by DGA CERTIFICATION in accordance with ISO 14001, you will uncover weaknesses in your environmental management system and create the basis for a continuous and verifiable process of improvement. You will reduce environmental risks, conserve natural resources and improve your environmental performance. Active and effective environmental protection requires not only technology, but also an effective environmental management system. This is an increasingly important factor for competitive success.

BENEFIT OF ISO 14001:2015 CERTIFICATIONv Reduce emissions, waste and wastewater.

v Save money through the targeted use of resources.

v Reduce your environmental impact and improve your legal security.

v Ensure compliance with the requirements of both customers and authorities.

v Promote environmentally conscious behavior among your employees.

v Improve your image with customers, partners and the public.

v Achieve your own environmental goals and continuously improve your environmental performance.

v Identify sources of error at an early stage and can eliminate them.

v Receive international recognition for your operational environmental protection system.

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ISO 22000:2005 Certification (FSMS)

.ISO 22000:2005 is a food safety management for organizations involved in food chain. This standard specifies the requirements for food safety management system where an organization in food chain needs to demonstrate its ability to control the food related hazards. This standard was prepared by Technical Committee ISO/TC 34, Food products.

Food safety is related to the presence of food-borne hazards in food at the point of consumption. As the food safety hazards, can occur at any stage of the food chain, adequate control throughout the food chain is essential. Thus, food safety is ensured through the combined efforts of all the parties participating in the food chain. This International Standard specifies the requirements for a food safety management system that combines the following generally recognized key elements to ensure food safety along the food chain, up to the point of final consumption.

This International Standard integrates the principles of the Hazard Analysis and Critical Control Point (HACCP) system and application steps developed by the Codex Aliment Arius Commission. By means of auditable requirements, it combines the HACCP plan with prerequisite programmers (PRPs). Hazard analysis is the key to an effective food safety management system, since conducting a hazard analysis assists in organizing the knowledge required to establish an effective combination of control measures.

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BENEFITS OF ISO 22000:2005 CERTIFICATION

v Competitiveness of competitors in creating marketing enables avoided.

v Employee awareness about hygiene and food safety allows.

v Food legislation and ensures regulatory compliance.

v Provides customer confidence and satisfaction.

v Within and outside the European Union provides ease of trading.

v Preventive rather than corrective methods to prevent loss of use of the product.

v Product quality is improved.

v Provides a general approach to safety issues.

v Specification and be in harmony with the legal regulations is evidence.

DGA CERTIFICATIONv Potential hazards are initially uncovered and resolved.

v Control food-borne hazards provides an affordable way.

v Process control and reduce the risk of producing defective products provide.

v Unsafe products reduce the risk of the production and sales.

v For quality control of the products produced, enabling migration preventive quality assurance.

v Reduce the risk of food poisoning and death ensures.

v Problems encountered in official control methods for minimizing the definitions.

ISO 13485:2016 CERTIFICATION (MDQMS)

ISO 13485:2016 specifies requirements for a medical device quality management system where an organization

needs to demonstrate its ability to provide medical devices and related services that consistently meet customer

requirements and regulatory requirements applicable to medical devices and related services. The primary objective

of ISO 13485:2016 is to facilitate harmonized medical device regulatory requirements for quality management

systems.

As result, it includes some requirements for medical devices and excludes some of the requirements of ISO 9001 that

are not appropriate as regulatory requirements. Because of these exclusions, organizations whose quality

management systems conform to this International Standard cannot claim conformity to ISO 9001 unless their

quality management systems conform to all the requirements of ISO 9001 All requirements of ISO 13485:2016 are

specific to organizations providing medical devices, regardless of the type or size of the organization.

benefits of ISO 13485:2016 (MDQMS)

DGA CERTIFICATIONv Increase access to more markets worldwide with certification.

v Outline how to review and improve processes across your organization.

v Increase efficiency, cut costs and monitor supply chain performance.

v Demonstrate that you produce safer and more effective medical devices.

OHSAS 18001:2007 CERTIFICATION

Sound occupational health and safety policies are essential for employees, but they are also increasingly important for your customers and other stakeholders. Occupational Health and Safety Management systems certification to OHSAS 18001 is a strong sign of your organization’s commitment to your employees’ health and safety.

Many organizations implement an Occupational Health and Safety Management System (OHSMS) as a fundamental part of their risk management strategy to address changing legislation and protect their workforce and other persons working under their control. OHSAS 18001 certification enables organizations to manage operational health and safety risks and improve performance.

OHSAS 18001:2007 Certification addresses the following key areas: -

Working with DGA CERTIFICATION to audit and certify your occupational health and safety system will promote a safe and healthy working environment. Demonstrate your commitment to employee health and safety with an OHSAS 18001 certification audit of your occupational health and safety management system.

DGA CERTIFICATIONISO 45001 – A New Standard for Occupational Health and Safety Management Systems. The International Organization for Standardization (ISO) is developing a new standard for Occupational Health and Safety Management

Systems, ISO 45001. The final version of the standard is planned for publication in Q4, 2016.

BENEFITS OF OHSAS 18001:2007 CERTIFICATION

v Hazard identification, risk assessment and determining controls

v Legal and other requirements

v Objectives and OHS program(s)

v Resources, roles, responsibility, accountability and authority

v Competence, training and awareness

v Communication, participation and consultation

v Operational control

v Emergency preparedness and response

v Performance measuring, monitoring and improvement

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ISO 27001:2015 CERTIFICATION (ISMS)

The ISO 27001 standard adopts a process approach for establishing, implementing, operating, monitoring, reviewing, maintaining, and improving an organization’s information security management system. ISO 27001 is the actual standard to which certification is measured. It sets out the requirements for an Information Security Management System (ISMS).

An ISMS is a systematic approach to managing the security of sensitive information - encompassing people, processes, IT systems and policy.

An ISO 27001 certificate demonstrates that you have taken necessary precautions to protect sensitive information against unauthorized access and changes. ISO 27001 certificates are issued by a third-party certification body and proves that your information security management system has been certified against a best practice standard and found compliant.ISO 27001 is the only auditable international standard which defines the requirements for an Information Security Management System (ISMS). The standard is designed to ensure the selection of adequate and proportionate security controls.This helps you to protect your information assets and give confidence to any interested parties, especially your customers. The standard adopts a process approach for establishing, implementing, operating, monitoring, reviewing, maintaining, and improving ISMS.ISO 27001 is suitable for any organization, large or small, in any sector or part of the world. The standard is particularly suitable where the protection of information is critical, such as in finance, health, public and IT sectors. ISO 27001 is also highly effective for organizations that manage information on behalf of others, such as IT outsourcing companies: It can be used to assure customers that their information is being protected.

Benefits OF ISO 27001:2015 (ISMS)

v COMPETITIVE ADVANTAGE - As information security is very important for any organization, ISO 27001 Certification will give you a competitive advantage when you are compared with others.

DGA CERTIFICATIONv DEMONSTRATING YOUR CAPABILITY - You will be able to make a public statement of capability

without revealing your security processes.

v MINIMIZING RISK - Ensures controls are in place to reduce the risk of security threats and to avoid system weaknesses being exploited. Less changes of loss / theft of information.

v COMPLIANCE WITH LEGISLATION - your organization comply with legislative requirements related to information security. You also comply with your buyer's information security requirements.

v SECURITY BECOMES AN INTEGRAL PART OF BUSINESS PROCESSES: - the As ISO 27001 certification has a information security management system approach, information security becomes part of you processes.

ISO 20000-1:2011 CERTIFICATION ( ITSM)

ISO 20000 is the world's first international standard for IT Service Management. ISO/IEC 20000 is an international IT

standard that allows companies to demonstrate excellence and prove best practice in IT management. The standard

ensures companies can achieve evidence-based 28benchmarks to continuously improve their delivery of IT services.

ISO/IEC 20000 was released in 2011 based on the IT infrastructure library (ITIL®) best practice framework, and

updated in 2011.

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The standard is intended for organizations who provide managed IT services such as infrastructure and/or

applications support; this can be both for external delivery e.g. to clients who have outsourced their IT support, as

well as for internal IT groups. A certificate issued by third party registrar to demonstrates that your IT management

system has been certified against requirements of ISO 20000 requirements. Implementation of ISO 20000-1 by setting

up of internal processes gives confidence to customers about the delivering capability through use of IT

infrastructure.

ISO/IEC 20000-1:2011 is the formal specification and defines the requirements for an organization to deliver managed

services of an acceptable quality for its customers.

BENEFITS ISO 20000 -1:2011 CERTIFICATION ( ITSM)

v Achieve international best practice standards of IT service management.

v Develop IT services that are driven by and support business objectives.

v Integrate people, processes and technology to support business goals.

v Put in place controls to measure and maintain consistent levels of service.

v ISO/IEC 2000 is compatible with ITIL to support continual improvement.

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ISO 28000:2007 Certification (SCSMS)

ISO 28000:2007 specifies the requirements for a supply chain security management system, including those aspects critical to security assurance of the supply chain. Security management is linked to many other aspects of business management.

Aspects include all activities controlled or influenced by organizations that impact on supply chain security. These other aspects should be considered directly, where and when they have an impact on security management, including transporting these goods along the supply chain.

It will also help your organization link security management to many other aspects of your business activities. Our ISO 28000 audit will look at all activities controlled or influenced by organizations that impact your supply chain security, including transportation of goods along the supply chain.

We can audit your organization’s systems against the ISO 28000 standard performing a gap analysis and if desired taking you through the full certification process.

BENEFITS ISO 28000:2007 CERTIFICATION (SCSMS)

v Allows security to be managed as a process so that the effectiveness of securitymanagement can be measured and improved.

v Allows management to focus resources and efforts on areas with high-risk concerns (through a security risk assessment).

DGA CERTIFICATIONv Allows management to benchmark its security management efforts with international standards.

v integrated enterprise resilience.

v Systematized management practices.

v Enhanced credibility and brand recognition.

v Aligned terminology and conceptual usage.

v Improved supply chain performance.

v Benchmarking against internationally recognizable criteria.

v Greater compliance processes.

HACCP CERTIFICATION

HACCP (Hazard Analysis Critical Control Point) is an internationally accepted technique for preventing microbiological, chemical and physical contamination along the food supply chain.

The HACCP technique does this by identifying the risks, establishing critical control points, setting critical limits, and ensuring control measures are validated, verified and monitored before implementation.

HACCP certification enforced by such agencies as the US Department of Agriculture's Food and Safety Inspection Service (FSIS) and the Food and Drug Administration (FDA), is a scientific process control system for eliminating contaminants at critical areas in the food production and distribution process. HACCP certification helps to prevent, as close to 100% as possible, harmful contamination in the food supply system.

Demonstrating a real commitment to food safety through HACCP compliance can also transform your brand and act as an effective entry-to-market tool, opening new business opportunities around the world.

Our global network of food experts carries out HACCP audits and helps you focus on the hazards that affect food safety and hygiene. It is then possible to systematically identify where the hazards are by setting up control limits at critical points during the food production process.

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BENEFITS HACCP CERTIFICATION

v Implement internationally recognized food safety hazard controls.

v Demonstrate your commitment to food safety.

v Give producers, stakeholders and suppliers confidence in your controls.

v Align HACCP with ISO 22000 to improve food safety management systems.

v Effectively manage food safety risks across the whole supply chain.

v Continually review and improve your system so it stays effective.

ISO 50001:2011 CERTIFICATION (ENMS)

ISO 50001:2011 gives organizations the requirements for energy management systems (EnMS). ISO 50001 certification is based on the management system model that is already understood and implemented by organizations worldwide. ISO 50001:2011 Energy management systems – Requirements with guidance for use is a specification created by the International Organization for Standardization (ISO) for an energy management system. The standard specifies the requirements for establishing, implementing, maintaining and improving an energy management system, whose purpose is to enable an organization to follow a systematic approach in achieving continual improvement of energy performance, including energy efficiency, energy security, energy use and consumption. The standard aims to help organizations continually reduce their energy use, and therefore their energy costs and their greenhouse gas emissions.

DGA CERTIFICATIONISO 50001 was released by ISO in June 2011 and is suitable for any organization – whatever its size, sector or geographical location

ISO 50001:2011 has been designed for implementation by any organization, whatever its size or nature of business / activities, regardless of its geographical location. This International Standard specifies requirements of an energy management system (EnMS) for an organization to develop and implement an energy policy, establish objectives, targets, and action plans, which consider legal requirements and information related to significant energy use. DGA is a leading ISO 50001 certification company in India & our ISO 50001 certificate is recognized worldwide. Contact DGA for ISO 50001 audit & certification services.

ISO 50001:2011 standard is also known as energy management system. ISO 50001 certification provides a framework for using energy efficiently.

BENEFITS ISO 50001:2011 CERTIFICATION (ENMS)

By achieving certification to this international, best-practice Energy Management standard, your organization will accrue some of the numerous benefits of ISO 50001, including;

v Reduced greenhouse-gas (GHG) emissions and carbon footprint. Compliance with this standard will allow you to meet current or future voluntary and/or mandatory energy efficiency targets or GHG emission reduction legislation.

v Increase energy cost savings for the organization by reducing energy costs via a structured approach to managing your energy consumption.

v Increased knowledge of equipment efficiencies. By integrating your existing management systems, you can align your Energy Management System (EnMS) with existing management systems for additional organizational benefits.

v Informed decision-making processes from system design through to operation.

v Increased energy awareness among staff members at all levels.

v Structured approach to the Right First Time methodologies.

v Improved corporate image and credibility with all stakeholders and customer.

v Enhanced security of energy supply as you will have identified your energy risk exposure in areas within the organization and commenced processes to reduce them.

v Improved operational efficiencies and maintenance practices.

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ISO/TS 16949 CERTIFICATION

The ISO/TS16949 was jointly developed by the members of the International Automotive Task Force (IATF) in close collaboration with the International Organization for Standardization (ISO). The aim was to combine the individual requirements of the four most common automotive standards in Europe and the USA - QS-9000, VDA 6.1, EAQF and AVSQ – into a single standard. This technical specification together with customer-specific requirements defines quality system requirements for use in the automotive supply chain.

The ISO/TS16949 standard, specifies the quality system requirements for the design, development, production, installation and servicing of automotive related products. Vehicle component manufacturers should achieve this standard to be able to supply to the world's largest automotive manufacturers.

The certification is widely sought by automotive product manufacturers because automobile giants like BMW, Volkswagens, Fiat, Ford, GM, and Japanese auto majors recognize it. ISO/TS16949 system is available to all automotive supply chain companies.

BENEFITS of ISO/TS 16949 CERTIFICATION

v When you have a technical specification for automotive supply chain, you are guaranteed easy marketing through any

source, the reason being any company would want to work with you because of your high standard of quality. Because of

this you would see more people wanting to work with you and lesser rejections on product quality.

v Better reputation: Since these standards are one that is a must in the industry, you would have the best reputation in the

market. Competitors and industry experts would look at you as a company that provides the best quality in the business.

v Better efficiency: With the advantage of having such ISO TS 16949 certification, you would have better

v efficiency within the system. This would reduce your losses and increase the profitability of the company.

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ISO 17712:2013 certification

International Standard ISO 17712, Freight Containers - Mechanical Seals, published in September 2010, Is the Third Generation Of 17712. The First Generation Was a Publicly Available Specification (PAS) Published In 2003; TheSecond Generation Was a Revision To ISO/PAS 17712 Published In 2006. The Generations Are Cumulative Except For Some Fine-Tuning of Earlier Work.

The International Organization for Standardization (ISO) Permits Its Technical Committees to Draft and Vote onPublicly Available Specifications (PAS) As, In Effect, A Kind of Interim International Standard. A PAS Is Faster to Approve Than a Formal Standard, But It Has a Limited Shelf-Life.

The First Generation: ISO Technical Committee (TC) 104, Freight Containers, Formed Working Group 8 (WG8), Mechanical Seals Late In 2002. Industry and Government Experts Concluded That an International Standard on Mechanical Security Seals Would Enhance Post-9/11 Cargo Security. Using ISO's PAS Procedures, ISO/PAS 17712 Was Finished Quickly. The PAS Focused on The Physical Parameters of Three Classes or Levels of Seal Barrier Strength: Indicative ("I"), Security ("S"), And High Security ("H"). The Barrier Strength of a Seal Was and Still Is Measured with Four Tests: Impact, Shear, Bend and Tensile Strength. The Test Values That Distinguished Between "I", "S" And "H" Classes Reflected Numbers in Use by Major Customs Authorities.

The Quality of Seals Used in International Trade Improved as Trade-Related Programs Encouraged or Required Use Of ISO-Compliant "H" Seals. Two of The Earliest Programs Were the US Customs-Trade Partnership Against Terrorism (C-TPAT) And the World Customs Organization's "Framework of Standards to Secure and Facilitate Global Trade."

ISO/PAS 17712:2003's Narrow Scope Reflected the Time-Urgency of Industry Stakeholders. It Was Clear That the Seal Suppliers' Security-Related Business Practices Were At Least As Important as The Physical Strength of a Seal. Seal Manufacturers and Distributors with Immature or Careless Security-Related Management Practices Could Effectively Compromise the Security of The Best Physical Seal Before It Was Shipped Out Of The Door.

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Benefits of ISO Pas 17712:2010

v Reducing shipping delays that result when seals are lost or broken.

v Speed up logistic procedures

v When checking seals for signs of tampering, tamper-evident seals should permit personnel, with the suitable training, to detect compromised seals more simply.

v Reduced possibility of cargo theft or tampering.

v Reduced possibility of unofficial material being inserted into containers or other tools of global traffic (IIT).

CE MARKING

The CE mark is a mandatory European marking for certain product groups to indicate conformity with the essential health and safety requirements set out in European Directives. The letters 'CE' are an abbreviation of Conformity European, French word for European conformity. The CE mark must be affixed to a product if it falls under the scope of 'New Approach' Directives of European union.

Without the CE marking, and thus without complying with the provisions of the Directives, the product may not be placed in the market or put into service in the fifteen member states of the European Union and Norway, Iceland and Liechtenstein. However, if the product meets the provisions of the applicable European Directives, and the CE mark is affixed to a product, these countries may not prohibit, restrict or impede the placing in the market or putting into service of the product.

Existing in its present form since 1985, the CE marking indicates that the manufacturer or importer claims compliance with the relevant EU legislation applicable to a product, regardless of where manufactured. By affixing the CE marking on a product, a manufacturer is declaring, at its sole responsibility, conformity with all of the legal requirements to achieve CE marking which allows free movement and sale of the product throughout the European Economic Area.

For example, most electrical products must comply with the Low Voltage Directive and the EMC Directive; toys must comply with the Toy Safety Directive. The marking does not indicate EEA manufacture or that a product has been approved as safe by the EU or by another authority. The EU requirements may include safety, health, and

DGA CERTIFICATIONenvironmental protection, and, if stipulated in any EU product legislation, assessment by a Notified Body or manufacture according to a certified production quality system. The CE marking also indicates that the product complies with directives in relation to 'Electro Magnetic Compatibility - meaning the device will work as intended, without interfering with the use or function of any other device.

Not all products need CE marking to be traded in the EEA; only product categories subject to relevant directives or regulations are required (and allowed) to bear CE marking. Most CE-marked products can be placed on the market subject only to an internal production control by the manufacturer (Module A; see Self-certification, below), with no independent check of the conformity of the product with EU legislation; ANEC has cautioned that, amongst other things, CE marking cannot be considered a "safety mark" for consumers.

Existing in its present form since 1985, the CE marking indicates that the manufacturer or importer claims compliance with the relevant EU legislation applicable to a product, regardless of where manufactured. By affixing the CE marking on a product, a manufacturer is declaring, at its sole responsibility, conformity with all of the legal requirements to achieve CE marking which allows free movement and sale of the product throughout the European Economic Area.

For example, most electrical products must comply with the Low Voltage Directive and the EMC Directive; toys must comply with the Toy Safety Directive. The marking does not indicate EEA manufacture or that a product has been approved as safe by the EU or by another authority.

v List of CE Marking Directives:

v - Active implantable medical devices 90/385/EEC - Airborne noise

- Appliances burning gaseous fuels 2009/142/EC - ATEX 94/9/EC

- Cableway installations for persons 2000/9/EC - Conventional rail

- Construction products 89/106/EEC - Dangerous substances

- General product safety 2001/95/EC - High-speed rail 96/48/EC

- Explosives for civil uses 93/15/EEC - EMC 2004/108/EC

- Hot-water boilers 92/42/EEC - Marine Equipment 96/98/EC

- In vitro diagnostic medical devices 98/79/EC - Lifts 95/16/EC

- Low voltage 2006/95/EC - Medical devices 93/42/EEC

- Machinery 2006/42/EC - Pyrotechnic articles 2007/23/EC

- Measuring instruments 2004/22/EC - Pressure equipment 97/23/EC

- Packaging 94/62/EC - Recreational craft 94/25/EC

- Personal protective equipment 89/686/EEC - Postal Services

- Simple pressure vessels 2009/105/EC - Toys 2009/48/EC

- Weighing Instruments 2009/23/EC - R&TTE 1999/5/EC

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Halal Certification

The term ‘Halal’ is an Arabic which literally means ‘lawful’ or ‘permissible’. In Islam, this term refers to many aspects of daily life, but in relation to the production of products such as food, drink, pharmaceuticals and cosmetics, it refers to the composition of the products and the environment in which they are produced. The ingredients used must be judged to be lawful according to the principles of Islamic law.

The most important principle relates to the slaughter of meat. Briefly, for slaughter of an animal to be considered ‘Halal’, the name of God must be invoked before the slaughter is carried outfit must be done with a sharp knife in one movement, severing the trachea, esophagus, both jugular veins and both carotid arteries. The animal must then be allowed to bleed out completely. Throughout the process, pain to the animal must be minimized.

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BENEFITS OF HALAL CERTIFICATIONv As a confirmation for Muslim customers that the food served is Halal and is in accordance with Islamic Law.v Assure customers that the food served is Halal and healthy and the premise's hygiene and sanitation

procedures are in top-notch.v Widen the range of customers by attracting Muslim customers and non-Muslim who are Halal consumers.v Increase a restaurant's revenue and enhance its marketability especially to Halal consumers.v If planning to export, the Halal certificate will help to assure Halal consumers in importing countries

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Kosher Certification

Kosher certification is a standalone international quality standard which is increasingly prevalent in the food ingredients and retail sector. We offer affordable kosher certification services to small mom-and-pop’s and start-up’s all the way to large international companies. We’re often asked about the cost of kosher certification and the technical requirements that are required for our services.

There are many company specific factors that determine both the technical viability and the cost of obtaining kosher certification. Considering this, we encourage you to contact us and allow us to provide you with a free and customized quote for our kosher certification services and help you to determine that your company will firstly, qualify and secondly.

In some companies where the final products may not be certified the manufacturer will nevertheless insist that all ingredients comply with kosher standards. Furthermore, in this age of rationalization of supply chains buyers are looking for fewer suppliers that can provide a wider range of ingredients. Those able to offer both kosher and non-kosher ingredients are more likely to win the business.

Fcc Certification

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The Federal Communications Commission established the regulations on electromagnetic interference under Part 15 of the FCC rules in 1975. After several amendments over the years, these regulations were reconstituted as the Declaration of Conformity and Certification procedures in 1998.

By the regulation, the FCC DoC certification mark is mandatory for devices classified under part 15(IT equipment like computers, switched-mode power supplies, monitors etc., television receivers, cable system devices, low-power transmitters, un-licensed personal communication devices) and part 18 (industrial, scientific, and medical (ISM) devices that emit RF radiation) of the FCC regulations.

The certification mark is a stand-alone logo (as shown above) for the part 18 class of devices while, for the part 15 class, along with the logo, the label should display other data viz, the trade name of the product, the model number, and information whether the device was tested after assembling, or assembled from tested components.[2][10]

As of January 2012, there are 279 test firms worldwide, accredited with the Commission who are qualified to issue the declaration of conformity certificate.[11]

Even though most of the nation’s exporting electronic equipment into the US market have their own standards for EMI as well as independent certification and conformity marks (e.g.: The CCC certification mark for China, the VCCI (Voluntary Council for Control of Interference) mark for Japan, the KCC mark by the Korea Communications Commission for South Korea, and the BSMI mark for Taiwan), most of the products still sold in these markets hold the FCC label. Electronic products sold in parts of Asia and Africa hold the FCC label even though it holds no legal significance, and also without any means to verify whether they actually conform to the specified standards

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GMP CERTIFICATION

Good manufacturing practice (GMP CERTIFICATION) guidelines provide guidance for manufacturing, testing, and quality assurance to ensure that a food or drug product is safe for human consumption. Many countries have legislated that food and pharmaceutical and medical device manufacturers follow GMP procedures and create their own GMP guidelines that correspond with their legislation.

A GMP is a system for ensuring that products are consistently produced and controlled per quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.

GMP covers all aspects of production from the starting materials, premises and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process - every time a product is made.

BENFITS OF GMP CERTIFICATION

v Manufacturing facilities must maintain a clean and hygienic manufacturing area.v Controlled environmental conditions to prevent cross contamination of food or drug product from

adulterants that may render the product unsafe for human consumption.v Manufacturing processes are clearly defined and controlled. All critical processes are validated to ensure

consistency and compliance with specifications.v Manufacturing processes are controlled, and any changes to the process are evaluated. Changes that affect

the quality of the drug are validated as necessary.v Instructions and procedures are written in clear and unambiguous language. (Good Documentation

Practices)v Operators are trained to carry out and document procedures.v Cross contamination with unlabeled major allergens is prevented.

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RoHS CERTIFICATION

RoHS, also known as Lead-Free, stands for Restriction of Hazardous Substances. RoHS, also known as Directive 2002/95/EC, originated in the European Union and restricts the use of six hazardous materials found in electrical and electronic products. All applicable products in the EU market after July 1, 2006 must pass RoHS compliance. RoHS impacts the entire electronics industry and many electrical products as well. This means all products must conform to strict standards, provide extensive compliance documentation, and ensure that electrical and electronic products sold in the EU do not contain lead, cadmium, mercury, hexavalent chromium, polybrominated biphenyls (PBBs), and polybrominated diphenyl ethers (PBDEs) above the legal threshold. Manufacturers, owners, retailers, and importers alike need to ensure that their products comply to be distributed and sold in the EU.

ROHS will reduce the need for special handling of electronic waste in the future, while WEEE will deal with both existing and future waste, diverting it from EU landfills and reducing the threat of soil and water contamination, as well as human exposure to toxic substances.

To obtain the certification, it is necessary to seek out a third-party company that provides test reports of the material, material declarations directly from the supplier and what is known as a Declarations of Conformity. It is all about testing the material, making sure its housing, manufacturing and distributing is aligned with the set forward regulations of ROHS,When working with these third-party organizations, they test the presence of different chemical compounds and components, including lead, mercury, cadmium, hexavalent chromium, polybrominated diphenyl ethers and polybrominated biphenyls.

Benefits of rohs certification

v Demonstrates compliance to the UK RoHS enforcement agencyv Demonstrates best practice to UK and European industryv Builds confidence throughout the supply chainv Reduces overall RoHS testing costsv Helps sell products and increase profitsv Provides certification by a trusted, independent body

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C-TPAT CERTIFICATION

The advanced unlading process will be available to sea carriers in 10 seaports throughout the U.S. The process will potentially save time for sea carriers in the C-TPAT program and allow CBP to better focus our resources. See the FAQ and PowerPoint presentation in the sidebar for additional information about this exciting new benefit.

C-TPAT is but one layer in U.S. Customs and Border Protection’s (CBP) multi-layered cargo enforcement strategy. Through this program, CBP works with the trade community to strengthen international supply chains and improve United States border security. C-TPAT is a voluntary public-private sector partnership program which recognizes that CBP can provide the highest level of cargo security only through close cooperation with the principle stakeholders of the international supply chain such as importers, carriers, consolidators, licensed customs brokers, and manufacturers. The Security and Accountability for Every Port Act of 2006 provided a statutory framework for the C-TPAT program and imposed strict program oversight requirements.

BENEFITS OF C-TPAT CERTIFICATION

v C-TPAT certification results in a dramatically lower number of CBP inspections, resulting in reduced border delay times.

v Eligibility for the FAST program.

v Priority processing for CBP inspections. (Front of the Line processing for inspections when possible.)

v Assignment of a C-TPAT Supply Chain Security Specialist.

v Potential eligibility for CBP Importer Self-Assessment program (ISA) with an emphasis on self-policing, not CBP audits.

v Opportunity to attend C-TPAT security seminars.

DGA CERTIFICATION

SA8000 CERTIFICATION

It was created in 1989 by Social Accountability International (SAI), an affiliate of the Council on Economic Priorities, and is viewed as the most globally accepted independent workplace standard. It can be applied to any company, of any size, worldwide.

The most widely recognized global standard for managing human rights in the workplace is Social Accountability International’s SA 8000:2014. It is an auditable standard, suitable for organizations of all sizes anywhere in the world, and provides a framework for assuring all your stakeholders that social accountability is being stewarded by your management.

SA 8000 certification addresses issues including forced and child labor, occupational health and safety, freedom of association and collective bargaining, discrimination, disciplinary practices, working hours, compensation, and management systems.

As well as setting workplace standards, worldwide, SA 8000 also embraces existing international agreements, including conventions from the International Labor Organization, the Universal Declaration on Human Rights and the United Nations Convention on the Rights of the Child.

BENEFITS OF SA 8000 CERTIFICATIONv Achieve best practice in ethical employment, trading and operations.

v Engage and motivate your employees with improved morale.

v Introduce greater transparency to the way you run your business

v Maintain existing business and attract new customers and investors.

v Gain recognition as a socially accountable organization.

DGA CERTIFICATION

BIFMA CERTIFICATION

BIFMA is the not-for-profit trade association for business and institutional furniture manufacturers. Since 1973, BIFMA’s role has been to sponsor the development and refining of current and future standards, educate on their importance and application, and translate their necessary complexity into more easily understood and implemented formats. We also monitor the state of the industry, serve as a forum for member cooperation and collaboration, interact with international counterparts, and advocate for regulatory conditions that foster value and innovation.

Benefits of bifma certificationv Boost customer confidence in the quality and reliability of your furniture.

v Place your products on the market as safe, sustainable and environmentally friendly.

v Gain the lead against the competition with a neutral environment label.

v Demonstrate your high-quality standards.

DGA CERTIFICATION

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EMAIL: - DGACERTIFICATION@GMAIL.COMWEBSITE: - WWW.DGACERTIFICATION.COM