Certification Services in Vikas Puri, Delhi

Owing to our immense expertise in this domain, we have carved a niche in the industry as the reputed service provider for Organic Certification Compliance service.

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;

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.

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. 

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.

• Brand Name: Shree Vinayaka Engineering Services
• Material: Copper, Metal
• Condition: New, Used
• Application: Welding Use
• Country of Origin: India

Preparation of PWPS, PQR, WPS. Services Welding Qualifications Trainings and Certification Services  Welding Processes SMAW,GTAW,GMAW,FCAW Training services  Maintenance and Repair Welding Training and Services. Welding Documentation Services

We are the service provider of iso 9001 ,iso 14001 ,iso 18001,iso 13485,iso 27001 ,iso 22000, ce certification,who-gmp,isots16949,haccp, rohs,sa 8000 & others certificate.

we are one of the most well-distinguished companies in the market that are into providing iso 9001:2015 certification consultancy services in new delhi, delhi, india. As an iso 9001 certified organisation you will have implemented quality management system requirements for all areas of the business, including: facilities people training services equipment iso 9001 certification & ukas accreditation when you are satisfied that your organisation is working within the guidelines of the quality management system, it is time to call in an iso 9001 certification body.  the audit can be conducted by a number of different certification bodies, however it is important to note that not all iso 9001 auditing organisations are ukas accredited.   continual assessment achieving certification to iso 9001 is the first step of a process of continual improvement that will provide your organisation with the necessary management tools to improve working practices.

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.

We provide iso 13485 certification services. the certification of a quality management system, specifically for medical devices to iso 13485 proves advantageous, and in many cases essential, for medical companies which export their products to global markets. Some of the additional requirements relate to design controls, process controls (including environmental controls), special processes, traceability, record retention, and regulatory actions, which are more critical for the medical device industry. an iso 13485 compliant management system adopt a risk management appoach which includes assessment to identify & estimate risk, uses risk controls and techniques with a view to eliminate hazardous situations throughout product realization. iso 13485: 2003 represents the requirements that medical device manufacturers must incorporate into their management systems. iso 13485:2003 specifies requirements for a 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 is to facilitate harmonized medical device regulatory requirements for quality management systems. As a result, it includes some particular 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 are specific to organizations providing medical devices, regardless of the type or size of the organization. 13485 dictates that risk management must be thoroughly documented and conducted throughout a product's entire lifecycle, from initial concept to delivery and post-delivery. whatever devices you produce, as a medical device manufacturer you have a responsibility to consistently deliver devices that are safe and effective. Iso 13485:2003 is the international standard recognized for medical device regulations around the world. iso 13485: 2003 has been harmonized against the three directives (medical devices, in-vitro diagnostic devices and active implantable devices) so certification to this standard by an international certification body such as smc automatically demonstrates compliance with specific clauses in the regulations.

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.

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

Many european directives stipulate that a ce mark has to be applied to the products in question. A ce mark on a product serves as a declaration to the authorities that the product • complies with all valid european regulations and • has undergone the specified conformity-assessment procedures. Who is responsible for attaching the ce mark to the product? the most important point is that the manufacturer is responsible for ensuring that the product complies with the european regulations and for attaching the ce mark to the product, irrespective of whether said manufacturer is based in or outside the european community. The manufacturer can appoint an authorised representative domiciled within the european community to perform these duties on the manufacturer's behalf. The ce mark should not be confused with marks such as the gs mark or the dguv test mark. Only in special cases has a product bearing the ce mark been tested by an independent testing and certification body - this is not indicated by the ce mark. In the case of the gs and dguv test marks, the production process is also inspected.

We are one of the eminent ISO Certification Providers in the country. Our company has a team of highly experienced and trained personnel hired by us after following stringing recruiting policies. Our team is well-versed in procedures of obtaining varied ISO Certifications. Our members are great at auditing and providing solutions to make your company achieved the desired certifications. We can carry out documentation, planning and other follow ups on your behalf. Contact us anytime of the year.

ISO refers to the International Organization for Standardization and enhances the value of your product or service internationally. ISO stands for International Organization for Standardization, and it is an independent international organization that sets different standards for goods/services. While the overarching body sets these standards, implementation and certification depend on local certifying bodies, which conduct audits in order to ensure compliance. Furthermore, while ISO certification remains voluntary for many sectors, some others may see it as a legal requirement, while some stakeholders may include a valid certification as a contractual prerequisite. ISO enhances global standardization for the quality specification for your products, services, materials, information and quality management. It brings more credibility to your products or services that your products or services meet the quality expectations of your customers. Register for our ISO certification package today, and our team of experts will spearhead efforts to get your product/service ISO certified and ensure that you get the least amount of headache from the entire procedure. Sign up now so that you can proudly showcase that your product meets the international standards! eStartIndia is the best legal and business services platform for services relating to ISO certification in India, offering a variety of registration services like Trade License registration, ISO certification, MSME registration, etc.

It is applicable to all organizations, regardless of size, which are involved in any aspect of the food chain and want to implement systems that consistently provide safe products. The means of meeting any requirements of iso 22000 can be accomplished through the use of internal and/or external resources. benefits of iso 22000 & haccp certification ã¢ï¿½â¢ enables organizations to demonstrate a commitment to food safety ã¢ï¿½â¢ to plan, implement, operate, maintain and update a food safety management system aimed at providing products that, according to their intended use, are safe for the consumer ã¢ï¿½â¢ to demonstrate compliance with applicable statutory and regulatory food safety requirements ã¢ï¿½â¢ to ensure that the organization conforms to its stated food safety policy ã¢ï¿½â¢ increase customer satisfaction through delivery of products that consistently meet customer requirements including quality, safety and legality ã¢ï¿½â¢ improved customer confidence leads to increased market share ã¢ï¿½â¢ all control measures are subjected to hazard analysis

With the increasing use of internet, there has been a considerable rise in the online institutions, online classes, etc. These helps in saving time and are beneficial for the individuals acquiring it. The online NIFM is an institution facilitating its students with pre-recorded online classes, so as to get informed about different aspects of the stock market, financial markets with the help of several beginners’ level or advanced level courses. Most of the courses offered by them are of short duration. The mutual funds with NSE certification prepare the individuals to have knowledge and awareness of the investment of funds. The students must be competent and computer friendly, so as to learn how to prepare for the mutual funds exam. While preparation for online exams, the students requires good study as well as internet and computer competence, so as to become successful and get good marks. Also, this course facilitates its students to prepare for mutual funds NSE exam for certification. The students pursuing the beginners level course of mutual funds study about different features of mutual funds, debt funds, taxation, liquid funds, etc. The mutual funds question answers can also be seen in this course. The students of any age can enroll in any of the courses anytime.

What is ISI Mark Registration? ISI Mark Registration is considered the most recognized sign of the quality of the India subcontinent. It is a sign of better quality that signifies that the product having an ISI mark complies with all the quality and safety standards and also safe for human consumption. Companies need to get their products certified for ISI Mark so that they could provide the best quality products to their customers to satisfy their needs as well as to win their confidence. ISI (Indian standards Institution) is a body set up under BIS (Bureau of Indian standards), formulated under the Indian constitution. It is a certification for industrial items in India. A body was set up at the time when India gained the freedom to create standards needed for profitable growth and maintaining quality in Industries production. However, after functioning for a couple of decades the Indian government decided to bring a lot of changes in their standardization system. Hence, the new body came in the year 1986 for the standardization of Indian industrial products which was called BIS (Bureau of Indian standards). The newly formed BIS (Bureau of Indian standards) took over ISI (Indian standards Institution). Since then it is doing a great job. BIS (Bureau of Indian standards) have also shifted their objectives from testing to industrial products to satisfy the consumers and also undertake various quality certification activities. You should also note that BIS (Bureau of Indian Standards) has established a chain of laboratories at various places all over the country in order to test the conformity of certified products. To test the conformity to the standards regular monitoring and inspection of the products manufacturing process, testing of samples drawn from the factory as well as the market is done.

pcc certificate attestation, Certificate Apostille Services

Who-gmp certification, who-gmp certification in delhi, who-gmp certification in india, who-gmp certification in noida, who-gmp certification in bhopal, who-gmp certification in indore, who-gmp certification in haridwar, who-certification in mumbai, who certification in pune, who-gmp certification in hyderabad, who-gmp certification in chennai, who-gmp certification in bangalore, who-gmp is an acronym for world health organization - good manufacturing practice is the specifications derived by world health organization. gmp refers to the good manufacturing practice regulations promulgated by the us food and drug administration under the authority of the federal food, drug, and cosmetic act (see chapter iv for food, and chapter v, subchapters a, b, c, d, and e for drugs and devices.) these regulations, which have the force of law, require that manufacturers, processors, and packagers of drugs, medical devices, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective. Gmp regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, mixups, and errors. This in turn, protects the consumer from purchasing a product which is not effective or even dangerous. Failure of firms to comply with gmp regulations can result in very serious consequences including recall, seizure, fines, and jail time. who gmp is part and parcel of quality system that encompasses manufacturing and testing of active food ingredients, pharmaceutical ingredients and products,medical devices, diagnostics, and medical devices. Gmp certification confirms the products’ identity, composition, quality, purity and strength which they represent in the market. Under it, there is a set of guidelines that offer a system of procedures and documentation by which the confirmation of the products are given. We offer consultancy on attaining gmp certification that will give your product a high boost in the market.

Electrical Power Quality Analysis Services Consultant, Industrial Energy Audit

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.

Being one of the superior service providers we also provide customized solutions for consulting &certification in India for FAMI QS Certification. FAMI QS is basically a European code of practice for Animal Feed Additive and Pre-mixture Operators (codes). This code is implemented to ensure the safety of feed additives and pre-mixtures. Moreover this code also applies to import of feed additive and pre-mixture operators from third world countries. This code basically made to ensure the hygiene feed additives and pre-mixtures. So we at, Aims Management Consultants is committed to provide value based consultant and services &solutions to the utmost satisfaction of our clients. In the addition, we are one of the pioneers FAMI QS Certification Consultants in India.

Iso 27001 is the international standard which is recognised globally for managing risks to the security of information you hold. Certification to iso 27001 allows you to prove to your clients and other stakeholders that you are managing the security of information you hold. Iso 27001:2005 (the current version of iso 27001) provides a set of standardised requirements for an information security management system (isms). The standard adopts a process approach for establishing, implementing, operating, monitoring, reviewing, maintaining, and improving your isms the iso 27001 information security management system (isms) standard provides a framework for information security management best practice that helps organisations: protect clients and employee information manage risks to information security effectively achieve compliance protects the company's brand image. benefits of iso 22000 certification ã��ã¯â¿â½ã��ã�â¢ã��ã�â¯ã��ã�â¿ã��ã�â½ã��ã¯â¿â½ã��ã�⢠to plan, implement, operate, maintain and update a food safety management system aimed at providing products that, according to their intended use, are safe for the consumer, ã��ã¯â¿â½ã��ã�â¢ã��ã�â¯ã��ã�â¿ã��ã�â½ã��ã¯â¿â½ã��ã�⢠to demonstrate compliance with applicable statutory and regulatory food safety requirements, ã��ã¯â¿â½ã��ã�â¢ã��ã�â¯ã��ã�â¿ã��ã�â½ã��ã¯â¿â½ã��ã�⢠to evaluate and assess customer requirements and demonstrate conformity with those mutually agreed customer requirements that relate to food safety, in order to enhance customer satisfaction, ã��ã¯â¿â½ã��ã�â¢ã��ã�â¯ã��ã�â¿ã��ã�â½ã��ã¯â¿â½ã��ã�⢠to effectively communicate food safety issues to their suppliers, customers and relevant interested parties in the food chain, ã��ã¯â¿â½ã��ã�â¢ã��ã�â¯ã��ã�â¿ã��ã�â½ã��ã¯â¿â½ã��ã�⢠to ensure that the organization conforms to its stated food safety policy, ã��ã¯â¿â½ã��ã�â¢ã��ã�â¯ã��ã�â¿ã��ã�â½ã��ã¯â¿â½ã��ã�⢠to demonstrate such conformity to relevant interested parties, ã��ã¯â¿â½ã��ã�â¢ã��ã�â¯ã��ã�â¿ã��ã�â½ã��ã¯â¿â½ã��ã�⢠to seek certification or registration of its food safety management system by an external organization, or make a self-assessment or self-declaration of conformity to iso 22000:2005.

ISO 14001 Certification, Iso 9001 Certification, Certification Services

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All kind of certificates   Iso, Trade mark, GMP, environment, medical eqipments, food safety, FASSAI etc...