ISO Certification Services in Delhi

Benefits of ISO 22000:2005 Certification Implementing ISO 22000 will bring the following benefits to your organization : An auditable standard with clear requirements which provides a framework for third-party certification Suitable for regulators The structure aligns with the management system clauses of ISO 9001 and ISO 14001 Enables communication about hazards with partners in the supply chain System approach, rather than product approach Applicable to all organizations in the global food supply chain Systematic management of prerequisite programmes Increased due diligence Dynamic communication on food safety issues with suppliers, customers, regulators and other interested parties signifies that it is a truly global international standard Provides potential for harmonization of national standards Covers the majority of the requirements of the current retailer food safety standards Complies with the Codex HACCP principles Provides communication of HACCP concepts internationally A systematic and proactive approach to identification of food safety hazards and development and implementation of control measures Resource optimization internally and along the food chain All control measures are subjected to hazard analysis Better planning-less post process verification Improved documentation.

Benefits of ISO 9001:2015 Certification Increases productivity and maximizes quality Increases revenue and improves employee morale and satisfaction Saves time and money Enhances ability to attract new customers that have adopted requirements for certification Improves accountability of management Increases employees' understanding of their roles in success of their work and the company Creates greater motivation and dedication

The ISO 13485:2016 Medical Certification specifies the requirements for the QMS for providing the details related to the provision of medical devices. The requirement for this certification is essential for all companies regardless of their size and employees working for them. When the requirement is solely applicable to medical devices, it automatically gets associated with the services offered by the organization as well. Shine Certification is aided by a team of professional consultants that leave no stone unturned for the client to acquire ISO 13485:2016 Medical Certification.

Use ISO 13485 : To establish a Quality Management System (QMS) that is oriented towards the design, development, production, and installation of medical devices and related services. To demonstrate your ability to supply medical devices and related services that meet customer expectations and comply with regulatory requirements. To evaluate how well your organization is able to meet customer expectations and comply with regulatory requirements. To become certified or registered. ISO 13485 is not a product standard. It’s a process standard. Therefore, it’s not enough to establish a Quality Management System (QMS) that complies with the ISO 13485 standard, you also need to comply with all relevant product and service oriented technical standards and regulations. ISO 13485 Vs ISO 9001 : ISO 13485 is based on the ISO 9001 Quality Management standard. Both standards are organized in the same way and use basically the same numbering system. In addition, most of the ISO 13485 requirements are taken directly from ISO 9001 without modification. However, some ISO 9001 requirements were modified and others were excluded. Of course, ISO 13485 also includes a special set of requirements specifically related to the supply of medical devices and related services. In general, ISO 13485 is made up of two kinds of requirements: old ISO 9001 requirements and new requirements that are specifically related to medical devices and associated services. ISO 13485 excludes ISO 9001 requirements related to continual improvement and customer satisfaction. Continual improvement is excluded because most medical device regulations require organizations to maintain their Quality Management Systems, not to improve them. And customer satisfaction is excluded because committee members thought it was too subjective. When ISO 9001 wants you to document a procedure, it also wants you to implement and maintain it. Section 4.2.1 of ISO 13485 expands on this idea by including requirements, activities, and special arrangements. More precisely : When ISO 13485 wants you to document a procedure, the standard also wants you to implement and maintain it. When ISO 13485 wants you to document a requirement, the standard also wants you to implement and maintain it. When ISO 13485 wants you to document an activity, the standard also wants you to implement and maintain it. When ISO 13485 wants you to document an arrangement, the standard also wants you to implement and maintain it. Whenever a procedure, requirement, activity, or special arrangement must be documented, it does so by explicitly asking you not only to document it but also to implement and maintain it. ISO 13485 also places a greater emphasis on the use of procedures to regulate and control how activities and processes should be performed. In this sense, ISO 13485 is somewhat more prescriptive than ISO 9001. ISO 9001 often leaves it up to you to decide how work should be controlled, whereas ISO 13485 seems to have removed some of this flexibility by insisting on the use of formal procedures. Since ISO 13485 is all about medical devices and related services, it of course adds many new requirements to address the specific needs of this industry such as ISO 14971 Risk Management.Possible exclusions : ISO 9001 says that you may exclude or ignore some requirements if you can justify doing so. You can exclude section 7 product realization requirements if you cannot apply them because of the nature of your organization and its products. Similarly, ISO 13485 2003 says that you can exclude section 7 requirements if they are not applicable in your situation and does not violate the organization's medical devices statutory regulations. You may also exclude section 7.3 design and development if official regulations allow you to do so and if you have made alternative arrangements that comply with these regulations. Occasionally ISO 13485 uses the phrase “if appropriate? or “where appropriate? When a requirement uses this phrase, you may ignore or exclude it if you can justify doing so. Whenever you decide to exclude or ignore an ISO 13485 requirement make sure that you’ve got a good reason. Make sure you can justify and explain why, and make sure this explanation is documented in your quality manual. How to develop a QMS :In order to become certified, you need to develop a Quality Management System (QMS) that complies with the ISO 13485 standard. But how do you do that? One common approach is to carry out a Gap Analysis. Such an analysis will identify the gaps that exist between the new standard and your organization's processes. Once you know exactly what and where your gaps are, you can take steps to fill them. And once all of your gaps are filled, your Quality Management System will be ISO 13485 compliant. By using this approach, you will not only meet the new ISO 13485 standard, but you will also improve the overall effectiveness of your Quality Management System. If you're currently ISO 13485:1996 or ISO 9001:2000 certified, you can call us to conduct Gap Analysis Tool on your Quality Management System to the new ISO 13485:2003 standard.Once we've completed the Gap Analysis and filled all of the gaps, you're ready to ask a Registrar to audit the effectiveness of your Quality Management System. If your QMS meets ISO 13485:2003 requirements then the Registrar will then issue an official certificate to you and record your achievement in their registration. 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.

• Type of Certification: New Certification
• Type of Certification: New Certification
• Document verification Mode: Online
• Target Location: India
• Mode of Report: Hard Copy

Title: Get the 100% Authentic ISO Certification Services With Advance Quality Solutions Are you looking forward to having authentic ISO certifications at a reasonable rate in Delhi? If yes, then no other company can offer you a better service than Advance Quality Solutions. Being one of the leading consultation-providing agencies, we offer extraordinary ISO certification services that hold immense significance in increasing the prospect of any business. At Advance Quality Services, we always strive to persuade the different needs of our clients and thus, modify our services as per the suitableness and needs of our clients. We almost provide all sorts of ISO certifications after following all the legal rules and guidelines. All our expert members are highly trained and possess special expertise in this sector and therefore can deal with all the aspects of ISO authentication. Contact us now to get 100% authentic ISO certification service without the fear of any forgery.

ISO originated from the union of two organisations – the ISO (International Federation of the National Standardizing Associations) and the UNSCC (United Nations Standard Coordinating Committee). In 1946 over 25 countries met at the Institute of Civil Engineers in London to create a new international organisation, where the objective was to ‘facilitate the international coordination and unification of industrial standards’ From this the new organisation ISO began operations in February 1947. The word ISO is derived from the Greek ISOS meaning ‘equal’. As the International Organization for Standardization would translate differently across different languages it was decided that the short form name for the organisation would be ISO. Today the ISO has grown to a confederation of delegates representing over 150 countries and has published over 16,500 international standards. They meet on a regular basis to further develop new and existing management standards.

Lms certifications was established in 2009 offers a very comprehensive and diverse range of technical services to their clients by providing diverse services in management systems-quality, environment, safety, food, information technology and social accountability. The iso certification services in delhi provides certifications, accreditations and training services to the clients.

Elevate your IT service management with ISO 20000 Certification Services. Ensure excellence in delivering quality IT services with our expert guidance through the certification process. Achieve ISO 20000 certification, showcasing your commitment to efficient service delivery, continual improvement, and customer satisfaction. Our comprehensive support helps align your IT services with international standards, enhancing operational efficiency and market credibility. Opt for ISO 20000 Certification Services to stay ahead in the dynamic IT landscape, foster customer trust, and drive continuous service excellence. Transform your IT operations with a globally recognized mark of quality and reliability.

Food safety is crucial and integral part of the food industry and the company must have the appropriate certification to be on par with industry set standards. B4Q Management Ltd based in Delhi provides dependable ISO 22000:2018 Certification Services for our valuable clients.Our certification services help our clients to carry our food hazards analysis and at the same time assist our clients to design effective operational programmes for added food safety for their food business. Our hired experts are committed and work hard to assist and guide our clients at any time for complete customer satisfaction. Our services are priced competitively and delivered within the promised timeframe.   Benefits form ISO 22000:2018 Certification Integrates the principles of Hazards Analysis and Critical Control Point (HACCP) system developed be Codex Alimentarius Commission. It combines the HACCP plan with prerequisite programme (PRPs) and operational PRPs. Requires that all Hazards that may be reasonably expected to occur in the food chain are identified, assessed and controlled. Can be applied independent of other management system standards or can be integrated with existing other management systems. Allows even small, tiny scale organizations to implement as externally developed combination of control measures. Intended for organizations seeking more focused, coherent and integrated food safety management systems. Emphasis on preventions of food safety hazards of all types. Ensures compliance with legislative and regulatory requirements. Provides for management of potential emergency situations & accidents that can impact food safety.

Get ISO certification within a week for enhancing your business with expert help and guide. If you want to know more call on below number- 8881-069-069  

• Country of Origin: India
• Payment Mode: Advance
• Type Of Ownership: proprietor
• Dose/Strength: 200 mg
• Usage/Application: Personal < Hospital < Clinical
• Packaging Size: 1x15

Brand name of this medicine is Pirfenex . Pirfenex  medicine contains generic Pirfenidone . Pirfenidone are available in form of Tablet. Each Coated Tablet contains 200Mg Pirfenidone. One Pack of Pirfenex 30 Tablets. Manufacturer & Marketed company name of Pirfenex  is Cipla Pharma Ltd, India.   USED - Pirfenex Tablet is used in the treatment of idiopathic pulmonary fibrosis.     Dosage- As directed by the physician.   Details- 1.         Brand name – Pirfenex 2.         Generic - Pirfenidone 3.         Strength – 200 Mg 4.         Dosage form – Tablets 5.         Used –  It is used in the treatment of idiopathic pulmonary fibrosis. 6.         Packaging – 30 Tablets 7.         Manufactured & Marketed By –  Cipla Pharma Ltd 8.         Delivery time – 4 to 7 days (worldwide) & 24 hours to 48 hours (India)   Delivery process - We can ship your medicine worldwide within 4-12 days through E.M.S. - Express mail service.   Warning: Pirfenex medicine  is a prescription drug and should be used under proper medical guidance and advice. Do not share the medicine with others, since they may be suffering from a problem that is not effectively treated by this drug.   • Keep all medicines out of the reach of children and away from pets, never share your medicines with others, and use this medication only for the indication prescribed.   • The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.   Notice: The above information is an educational aid only. It is not intended as medical advice for individual conditions or treatments. Talk to your doctor, nurse or pharmacist before following any medical regimen to see if it is safe and effective for you.   Before eating/consuming any medicine kindly do consult with your doctor / Medical adviser / Nurse / Hospital /medicine Institution / Health advisor or pharmacist/ medicine healer.   Do not indulge in self medication using internet information.   Self medication can be dangerous.

Contact us, if in case looking for ISO 18001 Occupational Health And Safety CertificationService. Our company is the dependable ISO 18001 Occupational Health and Safety Certification Service provider from Delhi (India).  We are backed by a team of experts and have all the resources needed for the process of developing OH & S management system certification program, independent audits of compliance-related processes & controls and reporting on results. Moreover, we promise to complete the Service within the promised time period.Details : QSC has the capability and resources to support companies throughout the process of developing an effective OH&S management system certification Program, performing independent audits of compliance-related processes and controls, and reporting on results. OHSAS 18001 is the International Occupational Health and Safety Management Standard. It provides a framework for the effective management of OH&S including all aspects of risk management and legal compliance. It addresses occupational health and safety rather than any specific product safety matters.

  Certification can be a useful tool to add credibility, by demonstrating that your offerings- be it products or services- comply with the norms of the industry. Well, we can help you with such concerns. At UIL, ours is a team of talented individuals, who work diligently to fulfil ISO certification needs of the clients. With our services, we help clients in maintaining standards that are mandated by the certification bodies. Not just this, we also assist in completing paperwork and other formalities. We are based in Delhi, India; feel free to contact us anytime.

• Usage: Valid for Govt Tenders
• Timeline: Within 1 day

All ISO Compliance Certifcations - ISO 9001/ ISO 14001/ OHSAS / ISMS 27001/ Energy Management / SA 8000

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.

• Time: 1 Working Days
• Payment Mode: Online / Offline
• Service Mode: Online / Offline

Documents required Business Registration Proof (Certificate of Incorporation/ GST Certificate/ MSME Certificate etc.) Two copies of sales bill/purchase bill Aadhaar Card and PAN Card Visiting Card/Letter Head   Whats included in package ISO Selection Consultation ISO Certification ISO Audit/Surveillance   ABOUT ISO CERTIFICATION (LOWEST PRICE IN INDIA) The International Organization for Standardization (ISO) management standards are a series of frameworks that help you run your business effectively. ISO certification is proof from a third party, such as ourselves that you comply with an ISO management standard. ISO certification gives your organization credibility. ISO (International Organization for Standardization) is a worldwide federation of national standards bodies. Member organizations collaborate in the development and promotion of international standards for technology, scientific testing processes, working conditions, societal issues and more. ISO and its members then sell documents detailing these standards. This approval is typically valid for a period of three years, after which the company must recertify that its procedures meet the current form of the standard. This process is to be monitored by the registrar during that period of time. IAF ISO: It is a global federation for all the accreditation bodies worldwide, which is known as International Accreditation Forum or IAF. The government and administrations approve work projects only to the IAF approved ISO certified companies as it is required quality audits at regular intervals. It’s costly as compare to NON-IAF. NON IAF ISO: It’s very less costly as company to IAF ISO and getting a non-IAF ISO certification is much feasible as it does not require quality audits at regular intervals. Small businesses with limited resources need not get IAF certifications. Such certification is mandatory mainly in case of the application for government tenders.   How ISO Certification Works Training - Our experts shall provide the training to the organisation staff to deliver the customer expectaion and all other requiste parameters to be filed as per ISO standards. GAP Analysis - We assess differences in performance of business operations to determine whether customers expectaion are being met and, if not, what steps should be taken to ensure they are met successfully. Documentation - Our experience consultants assist you prepare documentation for securing ISO certification as per the desired standrads and will continue update as per industry requirment. Audit - We also assist and provide the auditing and assurance services where third party audit is required to secure certification. Implementation - GAP Analysis, Training and Documentation is a part of ISO implementation. Our expert shall do all necessary activity to implement the ISO standard within the organisation. Certification - On after suscessful implementation of the ISO standard, our consultants shall assist you securing ISO certification from well recognised accredation body.   ISO Certification Key Advantages Brand Reputation - ISO Certification help organisation build its reputation amoung the market. Tender Eligibility - ISO certification required to qualify certain government tender eligibility. Increase Revenue - ISO Certification encourage customers to buy product and services which leads to increase in revenue. Improve Efficiency - Implementation of ISO standards helps organisation to run business operation smoothly which results in efficieny improvement. Better Quality - ISO Certification ensure the delivery of quality products and services to the customers. Global Presence - ISO Certification is global acceptable certification. Organisation certified with ISO recognised world wide.   Type Of ISO Certification ISO 9001 - Its a quality management system which enhance and ensure customer satisfaction with quality delivery of product and services. ISO 14001 - It sets out framework of an effective environmental management system for the organisation. ISO 45001 - It ensure organisation has effective health and safety management system. ISO 20000 - It helps framing best practice in IT & improvement in the delivery of IT services. ISO 22000 - This standards ensures customers that organisation has effective food safety management. ISO 27000 - This standard relates to information security management system (ISMS) which ensure best practice in terms of security. ISO 50001 - It sets out best energy management principles which state consuming energy efficiently helps company save cost as well as helping to utilize resources economically. CE Marketing - This marking ensure that electronic product has complied with the requirements of the applicable European health, safety, and environmental protection benchmarks. ISO 13485 - This is quality management system which ensure medical devices and related services consistently meet customer and applicable regulatory requirements.   DOCUMENTS REQUIRED FOR ISO 9001 REGISTRATION Business Registration Proof - A document proof of business required such as certificate of incorporation, GST certificate, MSME certificate, Trademark certificate, etc. Letter Head or Visiting Card - A Letter Head or Visiting Card of the business required for which you are looking for ISO registration. Sales and Purchase Invoice - A Sale and Purchase Invoice evidencing the nature of business activity for which you’re securing ISO 9001 registration.