'information security risks'

“License to operate in the International Feeds Sector.” FEED SAFETY CHALLENGE Feed 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+ certification Companies 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.

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EU Deforestation Regulation (EUDR) Consulting Services By Shark Certification Pvt. Ltd., Indore – Guiding You Toward Responsible Sourcing and Regulatory Compliance The European Union Deforestation Regulation (EUDR) is a game-changing directive that affects a wide range of industries sourcing commodities linked to deforestation. At Shark Certification Pvt. Ltd., we offer expert consulting services to help businesses across India and beyond understand, comply with, and implement EUDR requirements effectively. 🌍 What is the EUDR? The EUDR aims to eliminate deforestation from supply chains by requiring businesses to ensure that their imported or exported products are not linked to illegal deforestation or forest degradation. This regulation applies to commodities like soy, cocoa, palm oil, coffee, cattle, timber, and rubber—and extends to derived products such as leather, paper, and furniture. If your company trades with the EU or supplies to EU-based partners, EUDR compliance is not optional—it's essential. 🛠️ Our EUDR Consulting Services Shark Certification Pvt. Ltd. offers complete support for businesses affected by the EUDR. Our services are built around clarity, compliance, and sustainable growth: ✅ 1. EUDR Impact & Compliance Assessment We analyze your supply chain and business processes to evaluate how EUDR applies to your operations. Our assessment covers: Product origins and sourcing practices Supply chain traceability gaps Legal and compliance risks Documentation readiness ✅ 2. Strategy & Implementation Support We guide your organization in aligning with the EUDR through tailored implementation plans, including: Building traceability and tracking systems Revising procurement and supplier policies Supplier onboarding and risk evaluation ✅ 3. Due Diligence & Risk Mitigation The EUDR mandates strong due diligence mechanisms. We help you: Conduct risk assessments for high-risk supply chains Develop mitigation strategies Monitor ongoing compliance ✅ 4. Staff Training & Capacity Building Our specialized training modules help teams across departments understand: EUDR regulatory expectations Risk identification and documentation Day-to-day roles in maintaining compliance ✅ 5. Reporting & Documentation Support We assist in organizing and managing documentation needed to demonstrate compliance, including: Due diligence statements Supplier declarations Verification records for product origins and legality 🤝 Why Partner with Shark Certification Pvt. Ltd.? ✔️ Expertise in Global Sustainability Regulations ✔️ India-based, globally aligned consulting ✔️ Customized solutions for SMEs and large enterprises ✔️ Efficient implementation and audit readiness ✔️ Ongoing compliance support We work closely with manufacturers, exporters, importers, and suppliers to help them meet the requirements of the EUDR and remain competitive in environmentally conscious markets.

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Apply For USFDA Certification In Indore Looking for comprehensive certification solutions? Shark Certification offers a wide range of services, including FSSC, BRC, HALAL, KOSHER, NGMO, GMP, USFDA, and ORGANIC. Let us guide you through the process. About the U.S. FDA The U.S. Food and Drug Administration (FDA) is a key federal agency under the United States Department of Health and Human Services. As part of the federal executive structure, the FDA plays a vital role in safeguarding public health by regulating a wide range of products including pharmaceuticals, food items, cosmetics, and medical devices. The FDA is responsible for the approval and oversight of: New pharmaceutical products, including biologics Food and feed additives for humans and animals Color additives used in consumables and cosmetics Select categories of medical equipment and devices To ensure that products entering the U.S. market meet stringent quality and safety standards, the FDA also conducts inspections in manufacturing units located outside the U.S., including facilities in India that export drugs and food items to the American market. These inspections are based on Current Good Manufacturing Practices (CGMP) standards set by the agency. Compliance and FDA Inspections During inspections, FDA officials assess the level of compliance with CGMP guidelines. If any deviations or concerns are observed, they are documented in Form 483. This form outlines specific areas of non-compliance and is discussed directly with the management team of the manufacturing facility. Alongside the Form 483, the agency provides an Establishment Inspection Report (EIR), indicating whether any further action is necessary. Companies are expected to respond to the Form 483 within 15 working days. While the response is not legally required, submitting a detailed reply outlining corrective actions is highly recommended to avoid escalation. If the response is inadequate or if violations are severe, the FDA may issue a Warning Letter. In critical cases, enforcement actions such as import alerts, product approval delays, or even revocation of manufacturing licenses can follow. The FDA Approval Process For a drug or high-risk medical device to receive FDA approval, the manufacturer must demonstrate that it is both safe and effective for its intended use. While the FDA itself does not conduct testing, it rigorously reviews the data and clinical trial results submitted by manufacturers. Approval is granted only after a thorough review by a multidisciplinary team of FDA experts—including statisticians, biologists, chemists, and clinicians. Why FDA Compliance Matters for Indian Manufacturers The U.S. remains one of the largest and most lucrative markets for pharmaceutical products. Over the past few decades, Indian pharmaceutical firms have gained a significant presence in the U.S. generics space. To maintain and grow this market share, ongoing compliance with FDA regulations is crucial. Shark Certification Pvt. Ltd. – Your FDA Compliance Partner At Shark Certification Pvt. Ltd., we specialize in helping pharmaceutical and medical device companies navigate the complex regulatory landscape of the U.S. FDA. Our goal is to provide tailored, efficient, and value-driven solutions that reduce compliance risks and enhance operational excellence. Our team comprises seasoned professionals with deep experience in FDA regulations, global quality standards, and risk-based auditing approaches. We support clients from audit readiness to submission preparation—ensuring both compliance and business continuity. Our Core Services CGMP and Pre-Inspection Audits Pre-Approval Inspection (PAI) Preparation Quality Assurance and Control System Development 21 CFR Part 11 & GAMP 5 Compliance & Audit Support IT System Validation and Audit Services Quality Risk Management System Development Process Analytical Technology (PAT) & Quality by Design (QbD) Process Validation and Documentation USFDA Audit Readiness Training Regulatory Submission Support: 510(k), PMA, NDA, ANDA, IND, IDE, DMF, PAS Specialized Expertise Areas End-to-end Quality System Implementation & Gap Analysis Data Integrity & Compliance Audits Vendor and Third-Party Audits Good Clinical Practice (GCP) Audits Risk Assessments and Due Diligence Reviews FDA Form 483 and Warning Letter Responses GMP Compliance for Pharmaceuticals and Medical Devices Partner with Shark Certification Pvt. Ltd. With an unwavering focus on regulatory excellence and global health standards, Shark Certification Pvt. Ltd. is your trusted partner for U.S. FDA compliance. Whether you're preparing for your first inspection or responding to regulatory observations, we provide the guidance, expertise, and support needed to achieve and sustain compliance.

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Empowering Ethical Business Practices with SEDEX SMETA Audit By Shark Certification Pvt. Ltd., Indore In today’s global marketplace, ethical sourcing and transparent business practices have become key differentiators. At Shark Certification Pvt. Ltd., we help organizations align with internationally recognized ethical standards through guidance and support for SEDEX SMETA (Sedex Members Ethical Trade Audit). Understanding SEDEX and SMETA It’s important to clarify that SEDEX (Supplier Ethical Data Exchange) is not a certification body, and there is no official “SEDEX certification.” Instead, SEDEX provides a collaborative platform where businesses can manage and share data related to ethical performance across global supply chains. The SMETA audit methodology, developed by the SEDEX membership, is a recognized audit protocol designed to evaluate ethical business practices in four key areas: Labour Standards Health & Safety Environmental Management Business Ethics SMETA allows companies to undergo a single audit and share the results with multiple customers, reducing the need for repeated assessments and saving time and resources. Benefits of SMETA Audit Participation By conducting a SMETA audit and becoming a member of SEDEX, your organization can: Demonstrate compliance with ethical and social standards Meet legal, regulatory, and contractual obligations Boost supplier credibility and win customer trust Enhance access to global markets and export opportunities Increase productivity through improved working conditions Mitigate risks using SEDEX’s risk assessment tools Reduce audit fatigue by sharing reports with multiple clients Whether your customer is requesting an audit or you're proactively building a more transparent supply chain, SMETA adds measurable value to your business operations. SMETA Audit Types: 2-Pillar vs 4-Pillar There are two types of SMETA audits: 2-Pillar Audit: Covers Labour Standards and Health & Safety 4-Pillar Audit: Includes the 2-pillar components, plus Environmental Practices and Business Ethics The type of audit depends on customer requirements and the nature of your business. SMETA Audit Process with Shark Certification Pvt. Ltd. At Shark Certification Pvt. Ltd. in Indore, we provide comprehensive consulting and audit preparedness services for SMETA audits. Our step-by-step approach ensures a smooth and efficient process: Gap Analysis – Evaluation of current systems against SMETA criteria Documentation Review – Guidance on policies, procedures, and legal compliance Employee Training – Sessions to raise awareness across the workforce Mock Audit – Simulated audit to identify potential non-conformities Remedial Action Plan – Assistance in closing any gaps or findings Audit Coordination – Liaison with SEDEX-approved auditors and platform support Ongoing Compliance Support – Post-audit improvements and re-evaluation assistance Why Choose Shark Certification Pvt. Ltd.? ✅ Located in Indore, serving businesses across India ✅ Experienced consultants well-versed in SEDEX SMETA protocols ✅ Personalized services tailored to your business needs ✅ Transparent and reliable support throughout the audit lifecycle ✅ Cost-effective solutions for both SMEs and large-scale manufacturers ✅ Training and tools to help maintain long-term compliance Get Started with SEDEX SMETA Today If your customers are requesting ethical trade assessments or you're ready to elevate your sustainability credentials, let Shark Certification Pvt. Ltd. guide your journey. We ensure that your business not only meets SEDEX expectations but also stands out as a socially responsible organization in your industry. Contact us today to learn more about SEDEX SMETA audits, and how our expert consultants can support your success.

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HALAL Certification in Indore with Shark Certification Pvt. Ltd. Expand Your Reach. Strengthen Customer Trust. Meet Global Standards. Are you planning to expand into international markets or serve a wider consumer base, including the growing Muslim population? Shark Certification Pvt. Ltd. in Indore offers comprehensive HALAL Certification services that help businesses meet Islamic dietary laws and gain a competitive edge. What is HALAL Certification? HALAL is an Arabic term meaning “permissible” or “lawful.” In the food and product context, HALAL Certification confirms that the items are produced, processed, and handled according to Islamic law (Shariah). This applies not only to food but also to cosmetics, pharmaceuticals, packaging, and more. Why HALAL Certification Matters for Your Business Tap into a global consumer base of over 1.8 billion Muslims Meet export requirements for countries that mandate HALAL compliance Build credibility and consumer trust among Muslim and non-Muslim consumers alike Ensure transparency in sourcing, processing, labeling, and logistics Boost your brand value by showing a commitment to ethical and religious standards Industries That Benefit from HALAL Certification HALAL Certification is essential for a variety of sectors, including: Food and Beverage Manufacturing Meat and Poultry Processing Pharmaceuticals and Healthcare Cosmetics and Personal Care Products Hospitality and Catering Logistics and Packaging Steps to Get HALAL Certified with Shark Certification Pvt. Ltd. Initial Consultation We evaluate your business type, products, and markets to understand your specific HALAL requirements. Gap Analysis Our team assesses current processes to identify areas that need to be aligned with HALAL standards. System Development We help you build a HALAL-compliant system including ingredient sourcing, manufacturing practices, documentation, labeling, and hygiene protocols. Employee Training We train your staff to ensure full understanding and implementation of HALAL principles across your operations. Internal Audit A pre-audit is conducted to ensure readiness before the final certification audit. Third-Party Certification Audit We coordinate with accredited HALAL certification bodies to carry out the official audit and secure your certification. Certification Issuance On successful audit completion, your organization is issued a HALAL certificate, valid for a specified duration. Continual Compliance Support We provide ongoing guidance for surveillance audits, renewals, and system improvements. Why Choose Shark Certification Pvt. Ltd. in Indore? ✅ 25+ Years of Certification Expertise ✅ Trusted by Leading Brands Across India ✅ Affordable and Transparent Pricing ✅ 100% Success Rate in Certification ✅ Dedicated Consultant Support ✅ Fast Turnaround Time ✅ Customized Solutions for All Industry Sizes Benefits of HALAL Certification Increase customer trust and brand loyalty Access global HALAL markets with confidence Qualify for government and private tenders Improve internal systems and food safety protocols Demonstrate compliance with international standards Reduce risks of consumer complaints or regulatory non-compliance Start Your HALAL Certification Journey Today At Shark Certification Pvt. Ltd., we are committed to helping businesses in Indore and across India achieve global certification standards. With our HALAL Certification services, you can build a brand that’s credible, ethical, and future-ready.

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FSSAI Compliance Services in Indore By Shark Certification Pvt. Ltd. – Your Trusted Food Safety Partner Under Section 31(1) & 31(2) of the Food Safety and Standards Act, 2006, every Food Business Operator (FBO) in India is legally required to obtain FSSAI Registration or License—whether you're a street vendor or a multi-national food brand. At Shark Certification Pvt. Ltd., we offer complete FSSAI compliance services to help food businesses across Indore and India meet mandatory regulatory requirements with ease and confidence. Who Needs FSSAI Registration or License? The FSSAI License/Registration is mandatory for businesses including (but not limited to): Small vendors, hawkers, and temporary or permanent food stalls Dairy businesses and milk chilling units Edible oil and vegetable oil processing units Slaughterhouses and meat processing facilities Food manufacturers, processors, and packaging units Proprietary and novel food producers (with FSSAI product approval/NOC) Cold storage, warehouse operators, and transporters (including refrigerated vans, milk tankers) Wholesalers, distributors, marketers, and retailers Hotels (star/non-star), restaurants, bars, and food chains Canteens, caterers, messes, clubs, and food vending agencies Home kitchens, dabbawalas, banquet halls, and religious food arrangements Importers, exporters, and e-commerce food businesses Government departments, corporate food outlets, airports, seaports, railways, and bus depots Mid-day meal kitchens and public food distribution centers Our FSSAI Compliance Services Include: At Shark Certification, we offer end-to-end FSSAI compliance support for businesses of all sizes and industries: New FSSAI Registration / State License / Central License Renewal of existing Registration or License Modification of license details including product category, address, or business structure Annual Return Filing (Form D1 / D2) and related declarations Assistance in Revocation of Suspended Licenses FSSAI Certified Training for FBOs and staff by qualified food safety trainers Facility Hygiene Audits by certified auditors Pre-inspection Surveys to prepare for official FSSAI audits and fix gaps before inspection Consultation on Labeling, Packaging, and Legal Metrology Norms Timely Alerts and Reminders for license renewal and return filing Why Choose Shark Certification Pvt. Ltd.? Certified Experts with deep industry and regulatory experience Accurate and Error-Free Filing with proper due diligence Confidentiality and Data Security assured Local Presence in Indore for better accessibility and faster service Free Initial Consultation to assess your FSSAI readiness Customized Compliance Plans for startups, SMEs, and large enterprises Training and Support throughout the certification journey Renewal and Filing Alerts via WhatsApp, Email, and SMS Updated Insights and Newsletters for food businesses Contact Us Today Ready to get your FSSAI Registration or License in Indore or any part of India? Let the experts at Shark Certification Pvt. Ltd. guide you through every step—from documentation to audit support.

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Europe is a competitive but prize market, easier to access than ever before. Too many Indian exporters, especially small and medium sized enterprises, avoid it because the technical requirements for entry seem too complicated, too difficult, or too expensive. Indian manufacturers who have successfully accessed the European market know that the time to understand the European system is well worth the effort. The European Union alone is filled with affluent consumers, approximately 450 million of them. The European market is a large area that comprises more than 25 countries. 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.

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Get ISO Certified with Shark Certification Pvt. Ltd. – Indore’s Trusted ISO Consultants Shark Certification Pvt. Ltd. is a leading ISO consultancy firm based in Indore, offering end-to-end support to organizations looking to implement internationally recognized management systems and obtain ISO certifications. With an expert team and a client-focused approach, we simplify the certification journey for businesses of all sizes. We specialize in providing consultancy services for the following key ISO standards: ✅ ISO 9001:2015 – Quality Management System (QMS) ISO 9001 is the world’s most recognized quality management system standard. It provides a framework for businesses to ensure consistent product and service quality, enhance customer satisfaction, and continuously improve operations. Benefits of ISO 9001 Certification: Improved customer satisfaction and loyalty Streamlined operations and enhanced internal processes Increased marketability and credibility Better decision-making based on data and performance insights Stronger focus on risk management and continual improvement Our Services Include: Gap analysis and QMS implementation support Internal audits and training Preparation for third-party audits Complete documentation and process alignment Assistance in maintaining and renewing certification ✅ ISO 14001:2015 – Environmental Management System (EMS) ISO 14001 helps organizations manage their environmental responsibilities efficiently. It enables companies to reduce environmental impact, comply with regulations, and demonstrate a commitment to sustainability. Benefits of ISO 14001 Certification: Reduction in waste and resource consumption Compliance with environmental laws and regulations Enhanced environmental performance and reputation Improved stakeholder and public trust Identification of environmental risks and opportunities Our Services Include: Environmental impact assessment and EMS setup Compliance analysis and legal requirement mapping Documentation and procedural implementation Internal audits and corrective action guidance Audit preparation and certification support ✅ ISO 45001:2018 – Occupational Health & Safety Management System (OHSMS) ISO 45001 is an international standard that focuses on reducing occupational injuries and diseases. It helps businesses create a safe and healthy workplace for employees, contractors, and visitors. Benefits of ISO 45001 Certification: Enhanced employee safety and workplace morale Reduction in accidents, incidents, and legal liabilities Compliance with national and international safety regulations Cost savings through fewer disruptions and improved productivity A proactive approach to risk prevention and hazard control Our Services Include: Health & Safety risk assessments OHSMS framework development and policy creation Staff training and safety awareness programs Internal safety audits and compliance reviews Support through the certification and surveillance process Why Choose Shark Certification Pvt. Ltd. in Indore? Expert ISO Consultants with industry-specific knowledge Tailored solutions based on your organization’s size and operations Transparent process with end-to-end documentation support Affordable pricing and fast-track certification Ongoing support for audit preparation, renewals, and training Trusted by 1000+ organizations across sectors Let’s Get Started! If you're ready to elevate your business through ISO 9001, ISO 14001, or ISO 45001 certification, partner with Shark Certification Pvt. Ltd. – Indore’s trusted name in ISO consultancy.

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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 system Higher 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 benefits ISO 9001:2015 puts greater emphasis on leadership engagement Helps address organizational risks and opportunities in a structured manner Uses 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 continuity Addresses supply chain management more effectively Is more user-friendly for service and knowledge-based organizations Advantages: 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 processes Customer satisfaction – through delivery of products that consistently meet customer requirements More Specific Benefits Reduces cost Improves product reliability Better process control and flow Better documentation of the processes Greater employee quality awareness Increased Productivity Certification Procedure The Certification Procedure is a multiple-step process. The certification cycle is described briefly: Applying for Certification (Turnkey Project) Consultancy/ Documentation & System Development as per Standard Pre audit (optional) Certification audit – (Stage 1 + Stage 2) Issue of certificate on successful completion of certification audit Surveillance audits at defined period Recertification audit after 3 years

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