Quality Consultants Ajmer Road, Jaipur, Rajasthan

What is U.S FDA ? The Food and Drug Administration (FDA or USFDA) is a federal agency which is the part of the United States Department of Health and Human Services. It is one of the United States federal executive departments. The FDA evaluates and approves many different things, including: · new drugs, including biologics, · food additives for people and animals, · color additives in food, drugs, and cosmetics for people and animals, · some medical devices The U.S. Food and Drug Administration (FDA) is responsible for regulating medical devices used to diagnose, prevent and treat COVID-19, such as diagnostic tests, ventilators, and personal protective equipment (PPE) including surgical masks, face shields, respirators, gowns, and gloves. Personal Protective Equipment (PPE): Respirators, Surgical Masks, Gowns, Gloves, and More Personal protective equipment (PPE) refers to protective clothing, helmets, gloves, face shields, goggles, surgical masks, respirators, and other equipment designed to protect the wearer from injury or help prevent wearer exposure to infection or illness. PPE is commonly used in health care settings such as hospitals, doctor's offices, and clinical labs, as well as veterinary hospitals, food production facilities, and food service settings. When used properly, PPE acts as a barrier between infectious materials (such as viral and bacterial contaminants) and your skin, mouth, nose, or eyes (mucous membranes). The barrier provided by the PPE has the potential to block transmission of contaminants from blood, body fluids, or respiratory secretions when used properly. PPE may also protect patients who are at high risk for contracting infections through a surgical procedure or who have a medical condition, such as an immunodeficiency, from being exposed to substances or potentially infectious material brought in by visitors and health care workers.

SA 8000:2015 Certification ConsultantsThe SA 8000 certification is the Social Accountability System standard. It is applicable to companies of any size that wish to address the social and ethical aspects of their business. A Social Accountability System proves to customers that the company holds adequate provisions for the protection of workers' rights. Further, it ensures ethical production of all goods manufactured by the company.SA 8000 is the first auditable standard in this field. The initiative is based on the well-known ISO 9001/ISO 14001 certification structure, conventions of the International Labour Organization (ILO), the Universal Declaration of Human Rights and the UN Convention on the Rights of the Child. SA 8000 Key Requirements Be senior management led. Be focused on continuous improvement. Be focused on prevention rather than reaction. Be supportive of workers’ rights and workers participation. Be compliant with local laws/codes. Be compliant with local laws/codes. Be systematic in addressing problems-Car's Process. Benefits of SA 8000 to manufacturers and suppliers Marketing advantage – more demand and value for goods from socially. Responsible manufacturers/suppliers. Enhancement of company productivity. Compliance to the laws of the land. Improvement of relationship with the Govt., NGOs, trade unions. Better image and position in labour market.     Benefits of SA 8000 for the retailers Cost reduction in monitoring. Better corporate image. Increased value for the products. Trust building with the analysts and investors when evaluated against social performance. Role of ConsultantTo assist industries seeking for the SA 8000 Certification from beginning to the granting of certification. We provide SA 8000 certification consultancy in all over India including cities like Delhi, Mumbai,Chennai, Kolkata, Bengaluru, Ahmedabad, Hyderabad, Patna, Kanpur, Lucknow, Allahbad, Noida, Faridabad, Gurgaon, Jaipur, Ajmer, Jodhpur, Kota, Udaipur, Vadodara, Surat, Rajkot, Silvassa, Vapi, Pune. Aurangabad, Nashik, Goa, Daman, Diu, Raipur, Bilaspur, Bhubneshwar, Cuttack, Jamshedpur, Vishakhapattnam, Siliguri, Guwahati, Varanasi, Shillong, Coimbatore, Mysore, Chandigarh, Indore, Bhopal, Shimla, Jammu, Rudrapur, Haridwar, Gangtok. We provide  SA 8000 certification consultancy in all over India including states like Rajasthan, Punjab, Haryana, Jammu and Kashmir, Utter Pradesh, Uttranchal/Uttrakhand, Bihar, West Bengal, Assam, Orissa, Karnataka, Andhra Pradesh, Tamilnadu, Kerala, Goa,Daman and Diu, Gujrat, Madhya Pradesh, Chattisgarh, Tilangana, Pondicherry, Andaman and Nicobar, Manipur, Mizorum, Meghalaya, Lakshyadeep 

What are the aims and objectives of NABL...? National Accreditation Board for Testing and Calibration Laboratories (NABL) is an autonomous body under the aegis of Department of Science & Technology, Government of India, and is registered under the Societies Act. NABL has been established with the objective to provide Government, Industry and Society in general with a scheme for third-party assessment of the quality and technical competence of testing and calibration laboratories. Government of India has authorized NABL as the sole accreditation body for Testing and Calibration laboratories.In order to achieve this objective, NABL provides laboratory accreditation services to laboratories that are performing tests / calibrations in accordance with NABL criteria based on internationally accepted standard for laboratory accreditation ISO/IEC 17025. These services are offered in a non-discriminatory manner and are accessible to all testing and calibration laboratories in India and abroad, regardless of their ownership, legal status, size and degree of independence. What is laboratory accreditation...? The concept of Laboratory Accreditation was developed to provide a means for third-party certification of the competence of laboratories to perform specific type(s) of testing and calibration. Laboratory Accreditation provides formal recognition of competent laboratories, thus providing a ready means for customers to find reliable testing and calibration services in order to meet their demands. Laboratory Accreditation enhances customer confidence in accepting testing / calibration reports issued by accredited laboratories. The globalization of Indian economy and the liberalization policies initiated by the Government in reducing trade barriers and providing greater thrust to exports makes it imperative for Accredited Laboratories to be at international level of competence. Why is laboratory accreditation required...? Laboratory Accreditation provides formal recognition of competent laboratories, thus providing a ready means for customers to find reliable testing and calibration services in order to meet their demands. Laboratory Accreditation enhances customer confidence in accepting testing / calibration reports issued by accredited laboratories. Society also needs to know the technically competent laboratory in fields such as Medical, Forensic, Food Testing etc. The globalization of Indian economy and the liberalization policies initiated by the Government in reducing trade barriers and providing greater thrust to exports makes it imperative for Accredited Laboratories to be at international level of competence. What are benefits of accreditation...? Potential increase in business due to enhanced customer confidence and satisfaction. Savings in terms of time and money due to reduction or elimination of the need for re-testing of products. Better control of laboratory operations and feedback to laboratories as to whether they have sound Quality Assurance System and are technically competent. Increase of confidence in Testing / Calibration data and personnel performing work.Customers can search and identify the laboratories accredited by NABL for their specific requirements from the directory of Accredited Laboratories. Users of accredited laboratories will enjoy greater access for their products, in both domestic and international markets, when tested by accredited laboratories. What types of laboratories can seek accreditation...? The laboratories should be legally identifiable & appropriately registered. They can be a part of a big organization or an independent entity. NABL can provide accreditation to: Laboratories undertaking any sort of testing or calibration in the specified fields. Private or government laboratories. Small operations to large multi-field laboratories. Site facilities, temporary field operations and mobile laboratories.Which fields of testing and calibration are covered by NABL...? NABL Accreditation is currently given in the following fields:Testing LaboratoriesCalibration LaboratoriesMedical Laboratories Biological Electro-Technical Clinical Biochemistry Chemical Mechanical Clinical Pathology Electrical Fluid Flow Haematology and Electronics Thermal & Optical Immunohematology Fluid-Flow Radiological Microbiology and Serology Mechanical Histopathology Non-Destructive Cytopathology Photometry Genetics Radiological Nuclear Medicine (in-vitro tests only) Role of Consultant To assist laboratories seeking for the NABL Accreditation as per ISO 17025  from beginning to the granting of accreditation. We provide NABL accreditation consultancy in all over India including cities like Delhi, Mumbai,Chennai, Kolkata, Bengaluru, Ahmedabad, Hyderabad, Patna, Kanpur, Lucknow, Allahbad, Noida, Faridabad, Gurgaon, Jaipur, Ajmer, Jodhpur, Kota, Udaipur, Vadodara, Surat, Rajkot, Silvassa, Vapi, Pune. Aurangabad, Nashik, Goa, Daman, Diu, Raipur, Bilaspur, Bhubneshwar, Cuttack, Jamshedpur, Vishakhapattnam, Siliguri, Guwahati, Varanasi, Shillong, Coimbatore, Mysore, Chandigarh, Indore, Bhopal, Shimla, Jammu, Rudrapur, Haridwar, Gangtok. We provide NABL accreditation consultancy in all over India including states like Rajasthan, Punjab, Haryana, Jammu and Kashmir, Utter Pradesh, Uttranchal/Uttrakhand, Bihar, West Bengal, Assam, Orissa, Karnataka, Andhra Pradesh, Tamilnadu, Kerala, Goa,Daman and Diu, Gujrat, Madhya Pradesh, Chattisgarh, Tilangana, Pondicherry, Andaman and Nicobar, Manipur, Mizorum, Meghalaya, Lakshyadeep 

What is ISO 22163:2017The International Organization for Standardization has published guidelines to bring a quality management approach to the rail sector.ISO/TS 22163, Railway applications – Quality management system – Business management system requirements for rail organizations: ISO 9001:2015 and particular requirements for application in the rail sector, aims to help system integrators and equipment manufacturers in the rail sector make quality improvements through common best practices.The technical specification is a sector-specific application of ISO 9001:2015 and was developed in collaboration with the Association of the European Rail Industry to build on its industry standard.ISO/TS 22163 defines quality management system requirements for the rail sector that can be applied throughout the supply chain—including design and development, manufacturing, and maintenance.In October 2016, the Association of the European Rail Industry, UNIFE, announced the decision of Technical Committee 269 of the International Organization for Standardization (ISO) to replace the global standard for quality management systems in the rail industry – IRIS Rev. 02 – by a new ISO/TS 22163 version. Consequently, organisations certified according to IRIS Rev. 02 will have to undergo transition audits to update their certificates to ISO/TS 22163. ISO/TS 22163 will be based on the structure and requirements of the ISO 9001:2015 standard, which it will adopt in full, but comprises additional requirements for the rail industry. Deadlines and schedule Publication of the ISO/TS 22163 and the associated certification rules is scheduled for May 2017. Following the publication of the new standard, organisations are required to implement the changes in their quality management system prior to a transition audit. Certification auditors seeking to carry out audits according to ISO/TS 22163 are required to attend, and successfully complete, training supervised by UNIFE. On this background, July/August 2017 is a realistic timeline for the first transition audits. As IRIS Rev.02 certificates will expire after 14 September 2018, and all non-conformities need to be closed for all audits before a new ISO/TS 22163 certificate can be issued, the last transition audits should be completed by July 2018. Regulation for the auditing of remote locations/ support functions and extended workbenches/ site extensions Since the quality management system of ISO/TS 22163 takes an integrated approach to the organisations and/ or the production site, the transition of the quality management system to ISO/TS 22163 at remote locations/support functions and extended workbenches/ site extensions must be completed before the transition audit takes place. As was the case for former regulations, remote locations/support functions must be audited prior to the associated production site(s). This principle continues to apply for the transition phase from IRIS Rev. 02 to ISO/TS 22163.The new ISO/TS 22163: 2017 standard:Is published in May 2017 and replaced the existing IRIS Rev.2.01, till September  2018, covers all requirements of ISO 9001:2015 and has been built according to the High Level Structure, supplemented by existing and new additional mandatory and optional requirements of the rail industry especially also new KPIs,continues to be supported by the "IRIS Audit Tool" that is based on the new IRIS Assessment Sheet, composed by around 870 mandatory requirements, which are grouped into about 300 questions, as well as new KO-requirements (plus additional optional requirements), Requires the appraisal of the customer focus performance level,Requires introduction of turtle diagrams and applies the methodology of Process Effectiveness Assessment Reviews (PEAR) for some mandatory processes, Utilizes a maturity model for business management systems concluding your companies BRONZE-SILVER-GOLD rating.Role of ConsultantAssisting to client from beginning till certification that includes documentation, training and internal auditing.

What is ISO 9001:2015 Certification?ISO 9001:2015 is the latest revision of the ISO 9001 international standards that specifics requirements for a quality management system (QMS).  The requirements are specified within seven clauses: Context of the organization Leadership Planning Support Operation Performance evaluation Improvement Organizations will get certified to this standard in order to demonstrate their ability to consistently provide products and services that meet customer, statutory and regulatory requirements. Certification is granted by accredited certification bodies (registrars) that will audit an organization at planned intervals to confirm conformance to the ISO 9001:2015 standard.The standard can be applied to any organization. Its benefits include enhanced customer satisfaction, standardized processes, improved quality of products and services, and a culture of continuous improvement.Role of consultant Awareness Training to personnel on ISO 9001 Training on Internal Quality Auditor Documentation like SOP, Quality Manual Conducting Internal Audit Assisting organization throughout in the certification process   We provide ISO 9001 certification consultancy in all over India including cities like Delhi, Mumbai, Chennai, Kolkata, Bengaluru, Ahmedabad, Hyderabad, Patna, Kanpur, Lucknow, Allahabad, Noida, Faridabad, Gurgaon, Jaipur, Ajmer, Jodhpur, Kota, Udaipur, Vadodara, Surat, Rajkot, Silvassa, Vapi, Pune. Aurangabad, Nashik, Goa, Daman, Diu, Raipur, Bilaspur, Bhubaneshwar, Cuttack, Jamshedpur, Vishakhapatnam, Siliguri, Guwahati, Varanasi, Shillong, Coimbatore, Mysore, Chandigarh, Indore, Bhopal, Shimla, Jammu, Sri Nagar, Rudrapur, Haridwar, Gangtok.Overseas clients are in Singapore, Mauritius, Thailand, China, Fiji Island, Sri Lanka and NigeriaISO 9001:2015 specifies requirements for a quality management system when an organization: Needs to demonstrate its ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements, and Aims to enhance customer satisfaction through the effective application of the system, including processes for improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements. All the requirements of ISO 9001:2015 are generic and are intended to be applicable to any organization, regardless of its type or size, or the products and services it provides.

ISO/IEC 17025:2017, General requirements for the competence of testing and calibration laboratories, is the international reference for laboratories carrying out calibration and testing activities around the world.Producing valid results that are widely trusted is at the heart of laboratory activities. ISO/IEC 17025:2017 allows laboratories to implement a sound quality system and demonstrate that they are technically competent and able to produce valid and reliable results.ISO/IEC 17025 also helps facilitate cooperation between laboratories and other bodies by generating wider acceptance of results between countries. Test reports and certificates can be accepted from one country to another without the need for further testing, which, in turn, improves international trade.In order to reflect the latest changes in market conditions and technology, the new edition of the standard encompasses the activities and new ways of working of laboratories today. It covers technical changes, vocabulary and developments in IT techniques and takes into consideration the latest version of ISO 9001 on quality management.Role of ConsultantTo assist laboratories seeking for the Accreditation as per ISO 17025 from beginning to the granting of accreditation.

IATF 16949:2016 (1st edition) represents an innovative document, given the strong orientation to the customer, with inclusion of a number of consolidated previous customer specific requirements.ISO/TS 16949 (1st edition) was originally created in 1999 by the International Automotive Task Force (IATF) with the aim of harmonizing the different assessment and certification systems worldwide in the supply chain for the automotive sector.  Other revisions were created (2nd edition in 2002, and 3rd edition in 2009) as necessary for either automotive sector enhancements or ISO 9001 revisions.  ISO/TS 16949 (along with supporting technical publications developed by original equipment manufacturers [herein referred to as OEMs] and the national automotive trade associations) introduced a common set of techniques and methods for common product and process development for automotive manufacturing worldwide.Key BenefitsA commercial advantage during contract negotiations A clear focus on continual improvement, emphasizing defect prevention and reduction of variation   and waste Time and cost savings, by avoiding multiple customer specific certification audits The international recognition of the ISO/IATF 16949:2016 standard increases the credibility of     your organisation when bidding for global sourcing contracts or expanding your business locally. Gaining certification also helps you to reduce production variations and improve your   manufacturing efficiency which can positively impact your bottom line. Furthermore, ISO/IATF 16949:2016 helps create a common quality system approach to the entire supply chain (for suppliers/subcontractors) and facilitates access to the industry's best practices. IATF 16949 – New Quality Management Standard for the Automotive IndustryISO/IATF 16949, the automotive industry’s most widely used international standards for quality management, has been replaced with a new global industry standard by the International Automotive Task Force (IATF) called IATF 16949. IATF 16949:2016 was published by IATF on October 4, 2016 and and replaced ISO/TS 16949, defining the requirements of a quality management system for organizations in the automotive industry and will fully respect the ISO 9001:2015 structure and requirements. IATF 16949:2016 is not a stand-alone quality management standard, but is implemented as a supplement to, and in conjunction with, ISO 9001:2015.Below is a Review of New Requirements In IATF 16949:2016:Risk-related requirements to minimize the likelihood of failure during new program development Risk-based thinking to maximize the potential realization of planned activities Requirements to adopt a process to assess the risk of changes and take appropriate action Enhanced product traceability requirements to support latest regulatory changes Integration of many common industry practices previously found in customer-specific requirements. This to assure commonality throughout the industry and reduce the need for extensive customer-specific requirements in these areas Requirements for both first and second-party auditors, including a documented process to verify internal auditor and trainer competency Clarification of sub-tier supplier management and development requirements Addition of corporate responsibility requirements Addition of a product safety section to ensure intended performance during the entire product life cycle without causing harm or damage Requirement to assess manufacturing feasibility If applicable, requirement that organizations must have a warranty process that addresses and integrates all applicable customer-specific requirements and warranty party analysis procedures to validate No Trouble Found Embedded software requirements for product validation, warranty and troubleshooting of issues in the field The new IATF/TS-16949:2016 Standard and the accompanying ISO-9001:2015 base standard – the two are separate documents now. To be certified to the new standard, the manufacturing site and their RSLs will be audited to both ISO + IATF standard(s) Increased focus during audit on operational performance and customer feedback (customer scorecards/metrics) Role of ConsultantTo assist industries seeking for the IATF 16949:2016   from beginning to the granting of certifications. We provide IATF 16949:2016 certification consultancy in all over India including cities like Delhi, Mumbai,Chennai, Kolkata, Bengaluru, Ahmedabad, Hyderabad, Patna, Kanpur, Lucknow, Allahbad, Noida, Faridabad, Gurgaon, Jaipur, Ajmer, Jodhpur, Kota, Udaipur, Vadodara, Surat, Rajkot, Silvassa, Vapi, Pune. Aurangabad, Nashik, Goa, Daman, Diu, Raipur, Bilaspur, Bhubneshwar, Cuttack, Jamshedpur, Vishakhapattnam, Siliguri, Guwahati, Varanasi, Shillong, Coimbatore, Mysore, Chandigarh, Indore, Bhopal, Shimla, Jammu, Rudrapur, Haridwar, Gangtok. We provide IATF 16949:2016 certification consultancy in all over India including states like Rajasthan, Punjab, Haryana, Jammu and Kashmir, Utter Pradesh, Uttranchal/Uttrakhand, Bihar, West Bengal, Assam, Orissa, Karnataka, Andhra Pradesh, Tamilnadu, Kerala, Goa,Daman and Diu, Gujrat, Madhya Pradesh, Chattisgarh, Tilangana, Pondicherry, Andaman and Nicobar, Manipur, Mizorum, Meghalaya, Lakshyadeep 

Extended Producer Responsibility (EPR) Ministry of Environment, Forest and Climate Change rolled out the E-Waste (Management) Rules in 2016 to reduce e-waste production and increase recycling.Under these rules, the government introduced EPR (Extended Producer Responsibility), which makes producers liable to collect 30 per cent to 70 per cent (over seven years) of the e-waste they produce.EPR is a registration done under CPCB (Central Pollution Control Board) for channelization of E-Waste. EPR is applicable to all manufacturer, importer, producer, consumer, bulk consumer, dealers, e-retailer involved in manufacture, sale, transfer, storage and processing of e-waste or electrical and electronic equipments , including their components, consumables and spare parts. Liabilities ·         CPCB has allotted the liability to collect and recycle the E-Waste to the Producer itself. ·         Either the producer can fulfil the responsibility by itself or can engage a PRO (Producer’s Responsibility Organization) for fulfilment of his responsibilities. The PRO engaged should be CPCB authorized. ·         The producer (Manufacturer/Importer) has to submit its previous import/sales data according to which the targets will be allotted by CPCB. Further quarterly import/sales data needs to be submitted once the EPR is issued. ·         The producer needs to conduct 2 seminars yearly for general public awareness regarding the hazardous effects of E-waste and methods to properly channelize and dispose E-waste in an eco-friendly manner. Our Assistance in getting the EPR License Quality Consultant consists of a team of experts consultants who understands your business and provides you with the most satisfactory solution to your query regarding how to get an EPR certificate. Not only this, but we will assist you throughout the process of EPR certification because we care about our clients, that’s why we comprise all the resources and experts to provide 100% assistance. Also, we are action-oriented, thus, we will invest our sustain efforts in completing the EPR certification process immediately. To know more about how to get an EPR certificate, contact us immediately. Our team has provided exemplary services to our valuable clients by ensuring proper  coordination, follow-ups, and acknowledgment by keeping clients’ needs in mind. We provide end to end Assistance for services related to the Extended Producer Responsibility certificate: You can expect reliable and punctual filling of the application form. Our EPR certificate consultants will assist you in the process of documentation and evaluation. Our EPR certificate agents are equipped with the necessary resources to track your application. We will directly coordinate with CPCB officials for proper follows- up and acknowledgement to ensure the availability of all the documents or information whenever required by CPCB. We invest our sustained efforts to meet the startled querries or demand of CPCB.        

Country of Origin : India

What is BRC Certification?The BRC Global Standard for Food Safety is developed by food industry experts from retailers, manufacturers and food service organisations to ensure it is rigorous and detailed, yet easy to understand.First published in 1998, the Standard is now in its eighth issue and is well-established globally. It has evolved with input from many leading global specifiers.It provides a framework to manage product safety, integrity, legality and quality, and the operational controls for these criteria in the food and food ingredient manufacturing, processing and packing industry. The BRC Global Standard focuses on: The importance of management commitment. Hazard analysis and critical control point (HACCP) based food safety programmes. Quality management systems. Auditing good manufacturing processes – it's not just a paperwork audit. Auditing areas which often have the highest rate of product recalls and withdrawals, such as labelling and packing. Developing systems to reduce exposure to food fraud. Ensuring consistency of the audit process. Providing a BRC Global Standard that is portable enough to allow Additional Modules to be added to reduce audit burden. Promoting greater resilience, transparency and traceability in the supply chain. Role of consultantTo assist industries seeking for the BRC Certification from beginning to the granting of certification. We provide BRC certification consultancy in all over India including cities like Delhi, Mumbai, Chennai, Kolkata, Bengaluru, Ahmedabad, Hyderabad, Patna, Kanpur, Lucknow, Allahbad, Noida, Faridabad, Gurgaon, Jaipur, Ajmer, Jodhpur, Kota, Udaipur, Vadodara, Surat, Rajkot, Silvassa, Vapi, Pune. Aurangabad, Nashik, Goa, Daman, Diu, Raipur, Bilaspur, Bhubneshwar, Cuttack, Jamshedpur, Vishakhapatnam, Siliguri, Guwahati, Varanasi, Shillong, Coimbatore, Mysore, Chandigarh, Indore, Bhopal, Shimla, Jammu, Rudrapur, Haridwar, Gangtok. We provide BRC certification consultancy in all over India including states like Rajasthan, Punjab, Haryana, Jammu and Kashmir, Utter Pradesh, Uttranchal/Uttrakhand, Bihar, West Bengal, Assam, Orissa, Karnataka, Andhra Pradesh, Tamilnadu, Kerala, Goa,Daman and Diu, Gujrat, Madhya Pradesh, Chattisgarh, Tilangana, Pondicherry, Andaman and Nicobar, Manipur, Mizorum, Meghalaya, Lakshyadeep.Overseas clients are in Singapore, Mauritius, Thailand, China, Fiji Island, Sri Lanka and Nigeria

Association of American RailroadsThe Association of American Railroads (AAR) is an industry trade group representing primarily the major freight railroads of North America (Canada, Mexico and the United States). Amtrak and some regional commuter railroads are also members. Smaller freight railroads are typically represented by the American Short Line and Regional Railroad Association (ASLRRA), although some smaller railroads and railroad holding companies are also members of the Association of American Railroads. The AAR also has two associate member programs, and most associate members are suppliers to the railroad industry.We provide consulting services for the AAR (Association of American Railroads) Quality Assurance Program Certification as per standard M-1003. This certificate is required to supply the railway components to American Railways.Role of Consultant: Documentation, training and Internal Auditing.

The company offers services for acquiring NABL 17025 Certification, which is a certificate given by National Accreditation Board for Testing and Calibration Laboratories (NABL). NABL provides certification to the laboratories performing various perfection tests as per the criteria set by NABL. With the NABL Certification, laboratories get the recognition as an authorized laboratory for third party assessments, etc. We will offer you complete guidance in acquiring NABL 17025 Certification with complete authenticity. Our team of experts will do all the documentation work required for having NABL 17025 certification. Clients have shown complete trust in our services and have appreciated our endeavors. What Is NABL ? NABL stands for National Accreditation Board for Testing and Calibration LaboratoriesIt is an autonomous organization that comes under Department of Science & Technology, Government of IndiaNABL is a sole government authorized accreditation body in India for laboratoriesNABL offer accreditation and certification to the laboratories as per the set laboratory accreditation standard i.e. ISO/IEC 17025NABL offers its services in a non discriminatory manner not only to the laboratories based in India, but in abroad as wellNABL provides accreditation to the laboratories that are duly registered and legally identifiableIt offers accreditation to Medical Laboratories, Testing Laboratories and Calibration Laboratories Benefits Of Having NABL 17025 Certification It enhances confidence of the customer in taking services of the authorized laboratory and accepting testing reports issued by themMakes accredited laboratories competent at the international levelProvides formal recognition to the laboratories in government and private sectorSaves time and money for the customer as NABL 17025 certified laboratories eliminate the need of re-testingProvides listing to the laboratories in Accredited Laboratories directoryOffer better control on laboratory operation, thus, ensure satisfaction Why Us ? We offer reliable servicesSupport of qualified and experienced professionalsOur team is well versed with all the legal formalities required for acquiring certificationWe ensure authentic documentationAssure to complete the work and get certificate within the shortest possible timeEnsure to meet the satisfaction level of the customer