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Learning services for non-formal education and training – Basic requirements for service providersThe objective of this International Standard is to provide a generic model for quality professional practice and performance, and a common reference for learning service providers (LSPs) and their clients in the design, development and delivery of non-formal education, training and development. This International Standard uses the term “learning services” rather than “training” in order to encourage a focus on the learner and the results of the process, and to emphasize the full range of options available for delivering learning services.This International Standard focuses on the competency of LSPs. It is intended to assist organizations and individuals to select an LSP who will meet the organization’s needs and expectations for competency and capability development and can be used to certify LSPs.ISO 29990:2010 is an International Standard for providers of training and further training. It offers a certifiable and state of the art Standard according to ISO requirements for Management Systems. The Standard addresses – for the first time with international validity – all types of educational institutions.This includes single trainers, private seminar providers, organizations providing further training with courses, curricula and internal training as well as further training up to higher educational institutions and universities. The Standard has some congruent features with other management systems, above all with ISO 9001.ISO 29990 is basically subdivided into two areas: learning services (for example, these services include designing, providing and monitoring of learning services) and management at the learning service provider for example business planning, financial management, risk management as well as human resources management. This Standard is the first Standard for learning providers that is valid and applied on an international scale. The advantages for learning providers are transparency of their own services, international comparability and defined processes for quality assurance.BENEFITS of ISO 29990:2010Advantages for Learning Service Providers:-    Outstanding performance during tendering work from official bodies.    Globally marketability.    Enhancement in internal quality potential.    Transparently defined & documented processes.    Enthusiastic and active trained experts participation in the development.    Work on (PDCA) Cycle.Advantages for Learner:-    Adequate resources, including trainers with suitable competence, infrastructure and learning environment.    Evaluating criteria for Education.    Advanced & Authentic processes.    Transparency/comparability of services.    Assuring quality, transparency and comparability in educational institutions.Benefits for Global Cooperation    Base of development for international cooperation in the area of education and training    Globally comparable benchmarks for existence of quality.    No deformation of the globally competitive market.    Common unified standards/common understanding of quality
ISO 29990:2010
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“License to operate in the International Feeds Sector.”FEED SAFETY CHALLENGEFeed Safety and Quality are key issues for all companies handling feedstuffs and can have serious consequences when control is lost. A systematic approach is imperative for reducing risk and improving quality. Companies seeking to internationalize their business in Europe must be certified to a standard recognized by the GMP+ International (former PDV) organization. The GMP+ certification is also recognized by other feed certification schemes.Knowledge of GMP+ is spreading and the certificate is requested at a continuously greater extent throughout the world. The GMP+ regulations are in a process of continuous development and improvement and changes are relevant to all organizations in the international supply chain.WHAT ARE GMP+ STANDARDS BASED ON?The GMP+ standards have been developed to harmonize requirements for feed in order to ensure quality and safety throughout the entire feed chain. It is based on widely recognized principles of quality assurance, Hazard Analysis Critical Control Point (HACCP). Choosing which standard (B1, B2, etc.) and certification scope (production of feed materials, trade, etc.) depends on the organization’s role in the feed chain.GMP+B1 is mandatory for the production of compound feed, but can also be used for the production of feed materials and transport.B2 can be used for the production of feed materials and feed additives, while B3 is intended for trade and transshipment. Each of these standards is intended for different means of feed transport (e.g. B4.1 is intended for truck transport). All steps in the supply chain are thus covered by the given requirements.Advantages of GMP+ certificationCompanies benefit from GMP+ certification, because it:    is focused on quality management (ISO 9001) and risk management (HACCP);    provides access to supporting information and services, such as risk assessments, fact sheets, storing and sharing your monitoring data, newsletters, Early Warning messages etc);    Offers new sales opportunities and to a great degree, ensures the retention of current customers;    Guarantees the continuity of business operations, because the corporate structure is set up more efficiently and the costs and financial risks are limited;    Helps improve the company image and the reliability;    Makes your company part of a globally operating feed safety system (the GMP+ certificate is accepted internationally by about 12000 companies in 66 countries);    Is accepted by other (inter)national schemes;    Can easily be combined with multiple certifications (feed safety and sustainability);    Contributes to uniformity in the feed chain.
GMP+ Feed Safety Standards
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The Global Organic Textile Standard (GOTS) is recognized as the world’s leading processing standard for textiles made from organic fibers. It defines high-level environmental criteria along the entire organic textiles supply chain and requires compliance with social criteria as well.GOTS Version 5.0The new version of GOTS is a result of a comprehensive stakeholder input process in which various organizations with expertise in organic production, textile processing and social criteria participated. It follows the overall approach of GOTS to define high level verifiable environmental criteria throughout the entire processing chain of apparel and home textiles (including spinning, knitting, weaving, wet processing, manufacturing, and trading) made from a minimum of 70% certified organic fibers and requiring social criteria while still providing for a practical set of requirements that is technically achievable even in large scale industrial textile production and for mass market brands and retailers in order to achieve a considerable environmental and social impact in the textile industry.The implementation deadline for GOTS certified entities to fully comply with Version 5.0 is 1 March 2018.Benefit with GOTS Certification:There are numerous ways in which companies benefit from becoming certified to the Global Organic Textile Standard (GOTS). Below we list the top five reasons how and why becoming certified to GOTS supports a company’s business case for sustainability.RISK REDUCTION GOTS is a comprehensive risk management instrument for your supply chain.GOTS sets strict and extensive environmental and social criteria for the entire supply chainGOTS criteria are explicitCREDIBILITY Third party certification serves as independent external verification versus self-claims  Certification includes dual quality assurance – onsite inspection and product testing  Certification provides the credibility and verification of claims that investors,ü and the public, expect.EFFICIENCY AND PRODUCTIVITY GOTS’ wastewater management and other requirements result in improved eco-efficiencyGOTS’ social compliance management requirements results in improved socio-efficiencyGOTS certification facilitates sustainable supply chain management, cutting companies’ costs as they do not need to trace the whole supply chain themselvesINNOVATION AND DIFFERENTIATION GOTS certification can grant access to new markets, e.g. public procurementGOTS is explicitly recognized by governments and leading textile, sport, environmental, and organic organizations worldwideSustainability innovation provides added value over conventional products.SUSTAINABLE MARKET DEVELOPMENT Enables companies to be market drivers.Readies companies for the increasingly stringent regulatory climate.GOTS is recognized as the leading processing standard for textiles made from organic fiber worldwide.
The Global Organic Textile Standard (G
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Promoting organic production standards to meet consumer demandBUSINESS CHALLENGEIncreased cases of unsafe food due to over use of chemical fertilizers and chemicals in food production system, has created an increasing worldwide demand for organic food. The challenge facing the organic agriculture industry is to produce foodstuffs and agricultural products using methods, which respect the environment and animal welfare. Globally, these demands are defined by regulations, particularly in those countries, which consume organic products. The principal standards are NPOP standard (India Organic- APEDA), EU Regulation 834/2007 and the US National Organic Program (NOP). To take into account the regulations in place, the certification scheme depends both on the country of production and the country of destination.This certification is aimed at producer organizations or members of food industries who want to commercialize organic products for a particular market. The organic certification considered as a guarantee of quality and safety by the consumers.What is Organic Certification?Organic certification is a nationally and internationally recognized set of standards aimed at proving that agricultural and food products have been produced without the use of synthetic chemical products, while using methods, which respect the environment and animal welfare. Organic requirements involve a set of production specifications for growing, storage, processing, packaging and shipping. All organic assessment and qualification references require control and certification by an accredited independent body.Organic Certification Requirements vary from country to country and generally involve a set of production standards for growing, storage, processing, packaging and shipping that include:    avoidance of synthetic chemical inputs (e.g. fertilizer, pesticides, antibiotics, food additives), irradiation, and the use of sewage sludge;    avoidance of genetically modified seed;    use of farmland that has been free from prohibited chemical inputs for a number of years (often, three or more);    for livestock, adhering to specific requirements for feed, housing, and breeding;    keeping detailed written production and sales records (audit trail);    maintaining strict physical separation of organic products from non-certified products;    Undergoing periodic on-site inspections.Certified organic foods are not necessarily pesticide-free, certain pesticides are allowed.What are the key benefits?    Demonstrate Organic Standards compliance of products to clients (retailers, traders, importers)    Inspire consumer confidence    Ensure greater access to existing and target markets    Help protect the environment from harmful products and processes    Preserve animal welfareWHY CHOOSE SCPLWe are working with USOCA that is accredited for certification according to the NPOP, Swiss, European and NOP (USDA) organic production standard.With the NPOP, the client will also get certificate for Swiss and European Organic certification (EU Regulation No. 834/2007), which will make it recognized by all European Union member countries. In order to access the US market, you have to certify your products to the National Organic Program (NOP).
Organic Certification
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We provide consultancy service for GMP WHO certification to our clients. GMP (Good Manufacturing Practices) is a standard defined by WHO (World Health Organization). GMP WHO certification ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization.W.H.O. defines Good Manufacturing Practices (GMP) as “that part of quality assurance which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization”. GMP covers all aspects of the manufacturing process: defined manufacturing process; validated critical manufacturing steps; suitable premises, storage, transport; qualified and trained production and quality control personnel; adequate laboratory facilities; approved written procedures and instructions; records to show all steps of defined procedures taken; full traceability of a product through batch processing records and distribution records; and systems for recall and investigation of complaints.The guiding principle of GMP is that quality is built into a product, and not just tested into a finished product. Therefore, the assurance is that the product not only meets the final specifications, but that it has been made by the same procedures under the same conditions each and every time it is made. There are many ways this is controlled – controlling the quality of the facility and its systems, controlling the quality of the starting materials, controlling the quality of production at all stages, controlling the quality of the testing of the product, controlling the identity of materials by adequate labeling and segregation, controlling the quality of materials and product by adequate storage, etc. All of these controls must follow prescribed, formal, approved procedures, written as protocols, SOPs, or Master Formulae, describing all the tasks carried out in an entire manufacturing and control process.GMP covers all aspects of the manufacturing process including :Defined manufacturing processValidated critical manufacturing stepsSuitable premises, storage, transport, qualified and trained production and quality control personnelAdequate laboratory facilitiesApproved written procedures and instructionsRecords to show all steps of defined procedures have been takenFull traceability of a product through batch records and distribution recordsSystems for recall and investigation of complaints
GMP WHO Certification
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The ISO 14000 family addresses various aspects of environmental management The following are the composition of the standards:Environmental Management Systems (EMS)Environmental Auditing and Related Environmental Investigations (EA)Environmental Labeling (EL)Environmental Performance Evaluation (EPE)Life Cycle Assessment (LCA)Terms and Definitions (T&D)The ISO 14000 family includes most notably the ISO 14001 standard, which represents the core set of standards used by organizations for designing and implementing an effective environmental management system.ISO 14001:2015 CertificationThe ISO 14001:2015 certification provides a framework for a strategic approach to a company’s environmental policy, plans and actions. This provides the generic requirements for an environmental management system. Following are some of the essentials of our service.Environmental Management involves the management of all components of the bio-physical environment, both living (biotic) and non-living (abiotic). This is due to the interconnected and network of relationships amongst all living species and their habitats. The environment also involves the relationships of the human environment such as the social, cultural and economic environment with the bio-physical environment. These standards exist to help organizations minimize the negative impact of their operations on the environment.Following are the requirement of ISO 14001 organizationsEstablish an appropriate environmental policyIdentify the environmental aspects arising from the organization’s past, existing or planned activities, products and services, in order to determine the environmental impact of significance.Identify applicable legal and other requirements, to which the organization subscribesIdentify priorities and set appropriate environmental objectives and targetsEstablish a structure and programs to implement the policy and achieve objectives and meet targetsFacilitate planning, control, monitoring, preventive and corrective actions, auditing and review activities to ensure both that the policy is complied with and that the environmental management system remains appropriateBe capable of adapting to changing circumstancesAdvantages of ISO 14001:2015 CertificationProcess improvementEnvironmental cost reductionBetter relationships with regulatorsBetter relationships with insurers, investors, and financial marketsProduct improvementMarketing advantagesBetter control of liabilitiesReduced regulatory burdenProtection of company image and nameDemonstration of responsible managementThe ISO 14001:2015 Revision IntroductionThe main purpose of the revision is to provide a set of common and stable requirements for at least the next 10 years. This will be possible due to the requirement that all management systems standard use the same high level structure as a base. The purpose of ISO 14001:2015 is to provide organizations with a framework to protect the environment and respond to changing environmental conditions in balance with socio economic needs. It specifies requirements that enable an organization to achieve the intended outcomes it sets for its EMS. An approach to environmental management can provide top management with information to build success over the long term.The 2015 Revision Introduces New Concepts In The Management SystemAchieving a balance between the environment, society and economy is considered essential to meet the needs of the present without compromising the ability of future generations to meet their needs. Sustainable development as a goal for organizations is achieved by balancing the three pillars of sustainability.What are the main changes in ISO 14001?ISO 14001:2015 is structured around the High-Level Structure proposed in Annex SL for all ISO management systems. It includes, in addition to the usual 3 introductory clauses, 7 basic clauses common to all management system standards. They are: Context of the organization, Leadership, Planning of the EMS, Support, Operation, Performance evaluation and Improvement. They replace current EMS clauses 4.1, 4.2, 4.3, 4.4. 4.5 and 4.6. This structure is intended to provide a coherent presentation of requirements rather than a model for documenting an organization’s policies, objectives and processes.Even though the basic documentation control requirements remain the same, the organization can now decide what to document and how much. New ISO 14001:2015 shows that is not enough managing environmental aspects associated to the purchasing of products or services, but it’s necessary go a step further, influencing on environmental aspects related to its design, manufacturing processes and the further using of the products and services (life cycle).
ISO 9001, ISO 14001, or ISO 45001 cert
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Green building takes sustainable development concepts which can then be applied to a vast array of practices tied to constructionThere are many different approaches to take when maximizing the sustainability of a building’s design. Green doesn’t have to be about achieving the best green rating possible; every little green bit helps! Dovetail has put together a list of eight basic green building concepts to take into consideration.Important Areas to Consider When Building GreenClimate and LocalePeople MatterThink SmallCool Naturally and Heat EfficientlyGo NativeOld Before NewSustainable MaterialsInsulate and Ventilate
Green Building Concepts
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The ISO/TS 16949 was jointly developed by the International Automotive Task Force (IATF) members and submitted to the International Organization for Standardization (ISO) for approval and publication. The document is a common automotive quality system requirements catalog based on ISO 9001:2008, and specific requirements from the automotive sector. It’s  first edition was published in March 2002 as ISO/TS 16949:2002. This document, coupled with customer-specific requirements defines quality system requirements for use in the automotive supply chain.About 30 percent of the more than 100 existing automobile manufacturers affiliate the requirements of the norm but especially the large Asian manufacturers have differentiated, own requirements for the quality management systems of their corporate group and their suppliers. The requirements are intended to be applied throughout the supply chain. For the first time vehicle assembly plants will be encouraged to seek ISO/TS16949 certificationThe IATF has developed a common registration scheme for supplier 3rd party registration to the ISO/TS 16949. The registration scheme includes third party auditor qualifications and common rules for consistent global registration. Some of the benefits of the IATF registration scheme include:Improved product and process qualityAdditional confidence for global sourcingReassignment of supplier resources to quality improvementCommon quality system approach in the supply chain for supplier/subcontractor development and consistencyReduction in multiple 3rd party registrations
ISO/TS 16949:2009 Certification
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The International Standards specify requirements for quality management systems where an organization needs to demonstrate its ability to consistently provide product that meets customer and applicable regulatory requirements and aim to enhance customer satisfaction through the effective application of the system, including processes for continual improvement of the system and the assurance of conformity to customer and applicable regulatory requirements.The ISO 9001 certification defines good management practices and aims at providing a global standard that spells out quality and trust. A Quality management system can be used by an company in any industry. Since the standard is neither industry- nor product-specific, it may be used by any organization that provides a product or service.The ISO 9001 standard enable company to develop a Quality Management System (QMS) to meet customer quality requirements while progressively improving operational processes. It provides company with a set of principles that ensure a common sense approach to the management of your business activities to consistently achieve customer satisfaction.What is quality management system?It is the much desired framework that is needed to monitor and improve performance in any specialized area of your business. It could improve the way your business operates or it could help you bring down your operating costs.Benefits of quality management systemHigher levels of efficiency:  With the ISO 9001 Certification, you can be assured of better performances within the company. Your employees would be working towards a common goal and this would increase the performance of each department.Better belief in the company:  Employees always want to work with the best quality standards in place.Better brand image: having the right brand image is an important part of every business. Having a QMS implemented would lead to a good brand image within the industry, clientele and your competitors.Why ISO 9001:2015 certification?ISO 9001:2015 is a standard that sets out the requirements for a quality management system. It helps businesses and organizations to be more efficient and improve customer satisfaction. This is generic standard can be deployed across all industries.ISO 9001:2015 now follows the same overall structure as other ISO management system standards (known as the High-Level Structure), making it easier integrate multiple management systems. Another major difference is the focus on risk-based thinking; the new version gives it increased prominence. ISO 9001:2015 brings a number of benefitsISO 9001:2015 puts greater emphasis on leadership engagementHelps address organizational risks and opportunities in a structured mannerUses simplified language and a common structure and terms, which are particularly helpful to organizations using multiple management systems, such as those for the environment, health & safety, or business continuityAddresses supply chain management more effectivelyIs more user-friendly for service and knowledge-based organizationsAdvantages:Greater Assurance of meeting objectives as risk based thinking applied all across in the organization.Integration of QMS into business processes, as accountability of QMS lies with top management.Clear strategic direction of an organization as context of the organization is part of QMS.Promotion of leadership across organization.More reliable Product/Services as risk based approach is used for more effective and efficient service/product provision processesCustomer satisfaction – through delivery of products that consistently meet customer requirementsMore Specific BenefitsReduces costImproves product reliabilityBetter process control and flowBetter documentation of the processesGreater employee quality awarenessIncreased ProductivityCertification ProcedureThe Certification Procedure is a multiple-step process. The certification cycle is described briefly:Applying for Certification (Turnkey Project)Consultancy/ Documentation & System Development as per StandardPre audit (optional)Certification audit – (Stage 1 + Stage 2)Issue of certificate on successful completion of certification auditSurveillance audits at defined periodRecertification audit after 3 years
ISO 9001:2015 QMS Certification
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