Certification Services in Janakpuri, Delhi

We provide haccp certification services. haccp is a preventative approach to food safety and pharmaceutical safety which addresses physical, chemical, and biological hazards as a means of prevention rather than finished product inspection. Haccp is compatible with management systems, such as iso 9001and certification is recognized worldwide by government food authorities and food businesses. background haccp was developed as a microbiological food safety system for astronauts at the beginning of the manned us space program. The pillsbury company, nasa and the us army laboratories at natick pioneered the original system. At that time food safety systems were based on end-product testing. Ensuring full safety required testing 100 percent of the product. The preventive food safety system was born to ensure high level of food safety without using the entire product. haccp principles, developed by the codex alimentarius of the world health organization, demand that organizations establish effective food safety systems through the application of a systematic approach to hazard and risk analysis. This standard is used in the food industry to identify potential food safety hazards, so that key actions, known as critical control points (ccp's) can be taken to reduce or eliminate the risk of the hazards. food safety and public health agencies recognize haccp as the preferred tool for food safety assurance and improving regulatory food standards. The food safety and inspection service of the us department of agriculture (fsis-usda) mandated haccp in meat and poultry processing in 1996. The food and drug administration (fda) later mandated haccp for seafood and juices. The world health organization (who) advises the incorporation of haccp into international and national food legislation to improve food inspection efficiency. benefits provides employees with an understanding of the importance of producing safe food reduces spoilage costs helps reduce and possibly eliminate food safety liabilities improves consistency in product quality and safety improves business that relies on compliance with haccp gives customers increased confidence in your food safety improves competitiveness and makes your company a supplier of choice

We provide reach certification services. the aim of reach is to improve the protection of human health and the environment through the better and earlier identification of the intrinsic properties of chemical substances. At the same time, reach aims to enhance innovation and competitiveness of the eu chemicals industry. The benefits of the reach system will come gradually, as more and more substances are phased into reach. the reach regulation places greater responsibility on industry to manage the risks from chemicals and to provide safety information on the substances. Manufacturers and importers are required to gather information on the properties of their chemical substances, which will allow their safe handling, and to register the information in a central database. The agency acts as the central point in the reach system: it manages the databases necessary to operate the system, co-ordinates the in-depth evaluation of suspicious chemicals and is building up a public database in which consumers and professionals can find hazard information.

Busigo Overseas delivers easy attestation services in Delhi. These services are performed by an expert team with vast knowledge and experience in the industry. Our experts use advanced techniques to make this service successful. In addition, we provide this service at an affordable cost. The original Indian document to be produced from the Embassies / Consulates in India in other countries has to be legalized. The document must be followed in order to legalize from the respective embassy procedure. First of all authentication of the document should be by the relevant satellitare department or department of human resources and then the legalization of the document by the Departments of Foreign Affairs in New Delhi. We are worldwide leaders in visa and certification, stamped and immigration with integral service records and immediate solutions for any obstacle to certification. In offering attestation services, our company has made an unbelievable success. These services are widely requested because of their versatility and reliability. Moreover, after knowing their budget requirements, we offer them to our customers. These facilities are available at most competitive rates for customers. The customer relies heavily on our services of certificate attestation. This certificate has the official mark and signature of the authorities of the respective countries and is one of the legal and basic formalities. Attestation makes a certificate valuable legally and is therefore very much needed by the consumer. We assume responsibility for certifying and providing certificates to our customers within a committed period. In offering attestation services, our company has made an unbelievable success. These services are widely requested because of their versatility and reliability. Moreover, after knowing their budget requirements, we offer them to our customers. These facilities are available at the most competitive rates for customers. As a market leader, we deliver a qualitative variety of certification services. We provide these certificate services within the timeframe requested by using advanced technologies. Furthermore, we sell these facilities at very fair prices.

Boost your business with ISO certification in India sitting at your home within a week with expert help and guide. This is a very important certificate for enhancing your business. 

ISO 14001 is an Environmental Management Standard (EMS). It defines a set of environmental management requirements for environmental management systems. The purpose of this standard is to help all kinds of organizations to protect the environment, to prevent pollution, and to improve their overall environmental performance. ISO 14001 certification provides an organization’s customers, suppliers, employees and other stakeholders with evidence of the operations commitment to environment protection.Since it was first published in 1996, ISO 14001 has rapidly become the most important environmental standard in the world. Thousands of organizations use it, environmentalists support it, and governments actively encourage its use. ISO 14001 applies to all types of organizations. It doesn’t matter what size they are or what they do.Benefits of ISO 14001 : ISO 14001 drives protection of environment and help organizations : Reduce costs and increase profit through reduced waste and energy, reuse and recycle through 3R concept. Optimize use of resources (electrical, water and materials). Increase competitiveness. Reduce costs as a result of potential lower insurance rates. Environmentally responsible and commitment to environment protection. Cost saving through improved efficiency and productivity. Boost company’s public image.   How to use ISO 14001 :If you don’t already have an Environmental Management System (EMS), you can use this ISO 14001 standard to establish one. And once you’ve established your EMS, you can use it to manage the environmental aspects of your organization’s activities, products and services, and to improve its overall environmental performance. Environmental performance is all about how well you manage and control your environmental aspects and the impact they have on the environment.You can also use this standard to demonstrate that you are doing everything you can to protect the environment and improve your environmental performance. You can demonstrate your organization’s commitment in several ways : You can simply announce to the world that your EMS complies with the ISO 14001 standard (if it actually does). You can ask your customers or other interested parties to confirm that your EMS complies with the ISO 14001 standard. You can ask an ISO 14001 registrar or external auditor to verify that your EMS complies with the ISO 14001 standard. ISO 14001 expects organizations to comply with all of the requirements that make up the standard. No exceptions. According to ISO, every ISO 14001 requirement must be built into every EMS. However, the size and complexity of Environmental Management Systems vary quite a bit.How far you go is up to you. The size and complexity of your EMS, the extent of your documentation, and the resources allocated to it will depend on many things. How you meet each of the ISO 14001 requirements, and to what extent, depends on many factors, including : The size of your organization The location of your organization. The scope of your organization’s EMS. The content of your environmental policy. The nature of your activities, products, and services. The environmental impact of your environmental aspects. The legal and other requirements that must be met.   Your general approach : If you don’t already have an EMS, ISO 14001 suggests that you start with a review of your organization’s environmental status. Your environmental review should : Identify your organization’s environmental aspects. Study normal and abnormal operating conditions, as well as accidents, disasters, and emergency situations. Identify the environmental aspects associated with all operating conditions and situations. Clarify the legal and other requirements that apply to your organization’s environmental aspects. Legal requirements include National and International as well as local and regional laws and regulations. Other requirements include agreements that have been established with governments, customers, community groups and others as well as commitments, guidelines, principles, or codes of practice that influence how your environmental aspects ought to be handled. Examine your organization’s current environmental management policies, procedures, and practices. Pay special attention to your organization’s purchasing and contracting policies, procedures, and practices. Define the scope of your EMS. When ISO 14001 asks you to define the scope of your EMS, it is asking you to define its boundary. You can choose to apply ISO 14001 to the entire organization or only to a specific operating unit or facility. Once you’ve made this decision, you’ve defined the scope or boundary of your EMS. Henceforth, all activities, products, and services that falls within this boundary must comply with the ISO 14001 standard.   Once you’ve considered the above factors, you can begin the development of your organization’s unique Environmental Management System. But if you’ve already established an EMS and you simply need to update it to meet the new standard, you need to do a Gap Analysis. A Gap Analysis will compare your current EMS with ISO’s new ISO 14001 standard. This comparison will pinpoint the areas that fall short of the standard (the gaps). Once you know where to focus your attention, you can begin to make the changes that are needed to comply with the new ISO 14001 standard.

What you will get? Book: NO Mock test: Yes (online mock test with approx 500 question answers) Certification: For preparation for NISM exam NISM Assesment Structure: Duration: 180 minutes No. of questions: 150 Total Marks: 150 Marks per question: 1 Passing score: 60% Negative Marking: Yes (25%) Certificate validity: 3 years

Iso 13485:2003, based on the iso 9001:2000 certification process model, suggests that the application and management of a system of processes is an effective way to ensure good quality management. All requirements of this international standard are specific to organizations providing medical devices, regardless of the type or size of the organization. the standard strongly infers that clients should consider using iso 9000:2000 to ensure understanding of the process model, definitions and other items of concern, too iso 13485 certification – benefits the benefits of an iso 13485:2003 certification compliant quality management system to the thousands of companies worldwide include: 1. recognition by regulators around the world of iso 13485:2003 as a good basis for addressing medical device design and manufacturing regulatory requirements 2. controlled consistency of manufactured products 3. managed productivity and efficiency, controlling costs 4. competitive advantage and increased marketing and sales opportunities. 5. improved customer perception of the organization’s image, culture and performance. improved communications, morale and job satisfaction – staff understand what is expected of them and each other.

Our world-leading certification services enable you to demonstrate that your products, processes, systems or services are compliant with national and international regulations and standards.

Get your product ce marked to explore international market ce marking is the symbol as shown on the top of this page. The letters "ce" are the abbreviation of french phrase "conformité européene" which literally means "european conformity". • ce marking on a product is a manufacturer's declaration that the product complies with the essential requirements of the relevant european health, safety and environmental protection legislation. • ce marking on a product indicates to governmental officials that the product may be legally placed on the market in their country. • ce marking on a product ensures the free movement of the product within the efta & european union (eu) single market (total 28 countries), and • ce marking on a product permits the withdrawal of the non-conforming products by customs and enforcement/vigilance authorities. ce certification ce certificate ce consultancy ce mumbai ce bangalore ce pune ce ce india ce marking ce mark ce certification ce approval, what is ce marking, ce mark certificate, notified body, certificate of conformity europe, ce mark consultants consultant consultancy certification ce marking ce approved logo ce marking mandatory conformity mark, ce marking ce testing ce marking information, about ce marking, ce mark, notified body bodies self certified certification, notified ce mark, eu conformity declaration, ce mark consultancy, ce marking advisory service, ce marking consultancy, europe machine safety legislation, ce mark consultants and ce marking, ce marking consultancy services, ce certification, ce mark helpdesk, consultants europe is a technical and legal organization specialized in the ce mark, ce marking, ce certification and authorized representation of products, ce marking design, technical file consulting group for ce mark ce testing, ce mark consultancy, ce marking services, ce mark logo, consultant certificate certification consultancy in ce markings ambala haryana delhi india ce mark consultant in mumbai, maharashtra marking services, ce marking service providers, ce marking mumbai baddi, gujarat - ahmedabad, surat, bhavnagar maharashtra - mumbai, nagpur service providers of ce marking assistance services delhi, chennai, hyderabad, ghaziabad, international, ahmedabad ce marking services, ce marking service providers, ce marking related to : consultants for ce, ce, certificate, ce consultancy, ce consultants, ce certificate, cemarking

Iso 22000 certification covers all the processes in the food chain that impact the safety of the end product. It specifies the requirements for a comprehensive food safety management systems as well as incorporating the elements of good manufacturing practices (gmp) and hazard analysis critical control points (haccp). This internationally recognized food safety standard should be used by all organizations in the food supply chain from farming to food services, processing, transportation and storage through packaging to retail. You can demonstrate your commitment to food safety and improve your competitive position with an audit from our global network of food safety specialists. Developed in 2005, iso 22000 certification creates a single food safety standard that harmonizes the various national standards into one easy to understand set of requirements that are simple to apply and recognized around the world. Iso 22000 is the core basis of fssc 22000, the global food safety initiative recognized standard which additionally addresses the specific requirements of major retailers and global manufacturers. benefits from haccp / iso 22000 helps identify process improvements reduces the need for, and the cost of end product testing reduces the likelihood of product recall & adverse publicity facilitates better understanding of food packaging safety issues throughout the organization

We are offering iso certification services. The implementation of a qms should be a strategic decision of the organization implementing qms. Various factors influence the design and implementation of qms. These include – diverse needs and risks of organizations; particular goals and objectives; complexity of products and services provided;

However, the government has insisted on ISI marking of about 136 products which affect the health and safety of consumers or are products of mass consumption like LPG Cylinders, Food Colours and Additives, Cement, Packaged Drinking Water, etc.

S Marking is assurance that your brand reputation will not be put at risk by a product safety failure. In addition, because each "S Marked" product is independently tested, you don’t risk having your products taken off the market because they don’t meet market requirements. The S Mark provides the opportunity to leverage your company’s commitment to safety in your marketing efforts. Since CE marking does not require independent testing, critical consumers and retailers look for products with marks from impartial testing companies. In fact, surveys show that when consumers are aware of the difference between the S Mark and CE marking, nearly 80% say that the next time they buy an electrical product, it will be "important" or "very important" that it is S Marked. The S-Mark was originally developed in New Zealand and has become a leading assurance of product performance and safety. It is a powerful marketing tool that can give your product point of sale impact and differentiate it from the competition in advertising, tendering and sales presentations.

We are offering iso certification service. Iso 9001:2008 is an international standard related to quality management, relevant for any organization from all types of business sectors to be well established around the world as an invaluable quality management system. Provide a structure for taking an organized approach for managing your business processes to meet the quality requirements and also help your organization to improve your management processes to complete globally. Its goal is to provide quality management system that will be beneficial for your organization to help manage your business effectively and put in place best practice methodology. Iso 9001:2008 is based on following eight management principles: customer focus leadership involvement of people process approach system approach to management continual improvement

CE marking is mandatory for certain product groups within the European Economic Area (EEA; the 28 member states of the EU plus EFTA countries Iceland, Norway, Switzerland and Liechtenstein, plus Turkey). The manufacturer of products made within the EEA and the importer of goods made in other countries must ensure that CE-marked goods conform to standards

For the exporter, therefore, europe as a whole has become a market whose technical requirements have been greatly simplified. Before the creation of the european union, each country imposed its own technical requirements. Different standards and conformity assessment procedures forced exporters to target one or two countries only, or to forego exporting to europe altogether. The unification of these european countries into a european union, and the consequent harmonization of laws, standards, and conformity assessment procedures, changed all that. perhaps more importantly, iso 9001 certification is used extensively in europe as a condition of acceptance of a manufacturer's product or as a means of recognition of the manufacturer's credibility. It is important to note that a manufacturer with a quality system in place (such as iso 9001 qms) should not automatically assume that his or her products are ce compliant because of the quality system alone. The appropriate new approach directive(s) will prescribe the correct and full route to conformity assessment. the ce mark, which is affixed to a product or its packaging, is considered a proof that the product has met the requirements of the harmonized european standard, or directives; refers to communauté european. Translated from the french, this literally means european community. The european commission, which administers the program, describes the ce mark as a passport for goods to be sold freely within the internal european market. It is required by law if the product falls under one of the new approach directives. It is not a quality mark, nor is it a mark for consumers. Intended for member state authorities, it is the visible sign to those authorities that your product is in compliance with the new approach directives. All manufacturers are required to affix the ce mark to products that are governed by new approach directives. Ce marking on a product indicates to all authorities that the product is in compliance with the essential health and safety requirements of all directives that apply to the product. The first step to compliance is determining which directives apply to the product. A product may be regulated by more than one directive. The ce mark does not disclose which directive(s) or standards apply to the product, nor will it indicate the method of conformity assessment used to bring the product into compliance. This information is provided by other accompanying documents, such as the declaration of conformity. The manufacturer or the authorized representative affixes the ce marking to the product. It is not affixed by a notified body.

The CE marking services provided by our company ensure that the products of a company do comply with the CE marking and CE mark certification regulations. The experts of Aims Management Consultants are specialists of all the regulations of CE marking. Due to this expertise, it takes very les turn around time to certify a product by CE marking. We also offer our services at quite reasonable prices for everyone to avail theme easily. We have also gained the position of a leading CE mark consultancy in India. CE Marking CE Mark Overview To be sold within the European market, certain products require CE-marking. The CE mark declares that your product complies with the Essential Requirements of the applicable EU Directives. Applicable requirements are set forth in various European Directives that replace individual country safety standards. The Directives apply to products manufactured within but also exported to the European Union. The CE mark is placed on a product as the manufacturer?s visual identifier that the product meets the requirements of relevant European Directives. It is mandatory for a wide range of products sold within or exported to the European market. To facilitate free trade and ensure the safety of certain products, European countries have developed a series of standards, or Directives as they are called. Compliance is mandatory. It is a legal obligation on the part of the manufacturer or his agent. Penalties for failing to get CE-marking for a product can be severe. If you wish to sell your products within the European Union member states and the European Economic Area, the product in question must comply with the Directive(s). This also applies if you are a manufacturer who wants to export products into the European Member countries. The Directives replace individual country standards as they relate principally to the safety of these products. What products do the Directives cover? The Directives apply to a wide range of products. The most notable products that likely need CE-marking are : pressure equipment machinery of almost any description electrical and electronic equipment medical devices and equipment personal protective equipment equipment for use in potentially explosive environments There are certain exclusions, but if you manufacture any of the above types of equipment or products then one or more of the Directives almost certainly apply. Where is CE-marking required? CE-marking compliance is a legal requirement in the European Union member states and the European Economic Area countries. The countries are : Austria Belgium Cyprus Czech Republic Denmark Estonia Finland France Germany Greece Hungary Iceland Ireland Italy Latvia Lichtenstein Lithuania Luxemburg Malta Norway Poland Portugal Slovakia Slovenia Spain Sweden The Netherlands UK Other countries are likely to adopt the Directives in the future. EU Directives Directives apply to 99% of all industrial and domestic products sold in Europe; it is the distinctive CE mark that signifies compliance with the applicable Directives. Without the CE mark and the correct documentation, manufacturers and importers are at an immediate disadvantage when competing against compliant competitors. Complying with Directives The requirements of the Directives are to ensure that manufacturers have identified and addressed all aspects of design and manufacturing that could impact safety and the safe operations of the equipment. The actions required to become compliant with the Directives vary according to which Directive(s) apply and the type or classification of the equipment as defined by the Directive(s). However, there are some general steps you should follow : 1. Determine which, if any, EU Directives apply to your product(s), 2. Determine the extent to which your product already complies with the essential requirements of the Directives. 3. Choose conformity assessment routes. Depending on the nature of the equipment or product, you may be able to implement and declare compliance and affix the CE mark without assistance or service from an external company. A Notified Body is an independent body appointed by an agency within one of the European countries, usually governmental, as being capable of performing the duties of a Notified Body as defined by the Directives.

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Haccp can be considered a management system that addresses food safety through the analysis and control of biological, chemical, and physical hazards right from raw material production, procurement and handling, to manufacturing, distribution and consumption of the finished product. It's designed to be used in all segments of the food industry, and all the safety systems based on haccp principles have been successfully applied. Globally, food industries, as well as government agencies have accepted the seven principles of haccp, which are: analyze hazards determine the critical control points (ccps) establish preventive measures with critical limits for each control point establish procedures to monitor the critical control points establish corrective actions to be taken when monitoring shows that a critical limit has not been met establish procedures to verify that the system is working properly establish effective record keeping to document the haccp system advantages haccp offers a number of advantages focuses on identifying and preventing hazards from contaminating food enhanced assurance of food safety better management of resources timely response to problems is based on sound science permits more efficient and effective government oversight helps food companies compete more effectively in the world market reduces barriers to international trade

What is ISO Registration? In Today’s world, where the quality of standards plays an important role in the marketing of products and establishing the brand power or products market supremacy. Now, the question arises on how to judge the quality of the products? The answer is ISO (International Organization of standardization). ISO Certification certifies that a Manufacturing process service, management system or documentation procedure has all the requirements for standardization and quality assurance. International Organization for Standardization (ISO) is an independent, international and Non-governmental organization that develops a standard to assure the quality, safety, and efficiency of services, products, and systems. It is a non-governmental body which consists of a total of 148 countries as a member of countries and the Central secretariat of this body is located in Geneva, Switzerland. The objective of getting you ISO registered is mainly to advance the improvement of standardization in Technology. It improves the credibility of your business as well as helps you to achieve more business. There are a variety of standards that have been set up by ISO (International organization of standardization) but the most famous and mostly used standard are ISO 9000 and ISO 14000 The ISO 9000 standard is meant for quality management. The term quality management means activities organizations do in order to improve customer satisfaction by meeting their requirements and also improving the business. On the other hand, ISO 14000 is a family standard that is related to Environmental management. The primary concern for the environment refers to the activities the organization does to minimize the harmful effects of the activities of the business for the sustenance of the environment in the future.

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