About Us In South Asia Tüv Süd In India

Emily Johnson

-Mar 15, 2026, 4:37 PM

TUV SUD SOUTH ASIA PRIVATE LIMITED is a Private Limited Company and was incorporated on Aug 17, 1999 in India. It is registered at Registrar of Companies, ROC Mumbai. Its registered address is OFF SAKI VIHAR ROAD SAKI NAKA, ANDHERI (EAST), MUMBAI, Maharashtra, India, 400072. Its corporate identification number is (CIN) U74220MH1999PTC121330 and its current status is Active. Its industry classification as per MCA is technical Testing And Analysis.[Testing And Analysis Of Medical And Dental Specimen Are Classified In Class 8519]. It had a team size of 1825 employees as on Aug 31, 2025.

TUV SUD SOUTH ASIA PRIVATE LIMITED's last Annual General Meeting (AGM) was held on Jun 28, 2024 as per records from Ministry of Corporate Affairs (MCA). TUV SUD SOUTH ASIA PRIVATE LIMITED's authorised share capital is Rs. 300,000,000 and its paid up capital is Rs. 161,903,510. TUV SUD SOUTH ASIA PRIVATE LIMITED generated a revenue of Rs. 339Cr for the financial year ending on Mar 31, 2021.

TÜV SÜD South Asia was established as TÜV Bayern India, a branch office of TÜV Qualitats Management GmbH, in 1995. In 1999, it became a wholly owned subsidiary of TÜV SÜD Group. Today, TÜV SÜD South Asia is the leading certification, testing, auditing, inspection and training company with a strong presence in India, Bangladesh and Sri Lanka. TÜV SÜD South Asia has an extensive network of over 32 offices including 19 labs across the three countries. The company caters to a client base of over 10,000 companies across a wide range of sectors that include automotive, plant engineering, environmental technology, food safety, textile & leather, hard lines (toy testing, jewellery,... TÜV SÜD’s team of specialists, partner with clients to enhance their competitive strengths.

Key objectives at TÜV SÜD are to provide customers with solutions based on reliability, safety, quality, environmental protection as well as cost effectiveness. They understand the importance of impartiality and neutrality in carrying out their activities. Their management pays utmost heed to conflict of interest and ensures objectivity in all the activities that include management system certification, testing, inspection. TÜV SÜD South Asia was established as TÜV Bayern India, a branch office of TÜV Qualitats Management GmbH, in 1995. In 1999, it became a wholly owned subsidiary of TÜV SÜD Group. ACCREDITED BY: NABCB, DAKKZ, JAS-ANZ, ANAB WHAT IS IATF 16949?

IATF 16949 specifies the requirements of a quality management system for automotive production. Born from the need for a globally harmonised quality management system requirements document, IATF 16949 was published in October 2016. It supersedes the automotive standard ISO/TS 16949, which is no longer valid. IATF 16949 requirements include the following key aspects: Product safety Risk management and contingency planning Requirements for embedded software Change and warranty management Management of sub-tier suppliers Our free whitepaper provides further Information about... WHY IS CERTIFICATION TO IATF 16949 IMPORTANT? Obtaining the IATF 16949 certification demonstrates that your company has met extensive requirements to create a process of continuous improvement with an emphasis on defect prevention and reduction of variation and waste in the...

The technical specification is implemented for all branches of manufacturers and suppliers of products or production materials, services such as heat treatment or galvanising, and other products specified by automotive customers such as the... Certification to this technical specification is recognised by leading automotive manufacturers and OEMs. Most leading manufacturers will only work with companies that hold IATF 16949 certification, as they insist that suppliers adhere to the strict technical specifications laid out in the standard. Within the aviation, space and defence (ASD) industry, maintaining high safety levels is the foremost challenge. Even the smallest flaws in products or services can have fatal consequences. This has led to high expectations for quality, safety and reliability of parts, systems and services, which your company must achieve across the entire ASD supply chain.

Every organisation working in the ASD industry must therefore demonstrate its commitment to quality and reliability. WHAT IS AS/EN 91XX? The AS/EN 91XX (AS/EN 9100, AS/EN 9110 and AS/EN 9120) quality management systems are based on ISO 9001, with specific requirements on aviation, space and defence industries. Published by the International Aerospace Quality Group, the AS/EN 91XX standards unify various competing quality documentation and requirements to a standardised benchmark. The standards cover, but are not limited to: Configuration Management Project Management Risk Management Special Processes Control of work performed outside the supplier’s activities DEMONSTRATE YOUR COMMITMENT TO IMPROVING HEALTHCARE QUALITY Healthcare providers today rely on the ISO 9001 quality management system as a framework for success.

However, in order to truly achieve organisational efficiency, drive productivity and profitability, the continued reliance on ISO 9001 is insufficient. Healthcare providers seeking to differentiate themselves have to ensure that the core health-related issues such as patient safety and management of clinical risks are addressed and properly handled as well. This particular point is not covered under the ISO 9001 standards. WHAT IS DIN EN 15224? The DIN EN 15224 Quality Management System is a sector specific standard of quality management for healthcare organisations. It is based on the ISO 9001 standard and it includes tangible requirements for patient safety and management of clinical risks in the planning, realisation and management processes.

The DIN EN 15224 system brings together the advantages of ISO 9001 with comprehensive healthcare quality requirements. It defines issues ranging from the effectiveness and suitability of care, to the safety and reliability of care processes. In DIN EN 15524, there are 11 quality features which characterise the quality of healthcare and must be verified as part of a certification. The 11 central features of DIN EN 15224 are: Appropriate, correct care Availability Continuity of the care Effectiveness Efficiency Consistency Evidence-based, knowledge-based care Patient care, including physical and psychological integrity of the care Integration... ACCREDITED BY: (FSC) DEMONSTRATE THE RESPONSIBLE ORIGIN OF YOUR WOOD AND PAPER PRODUCTS The demand for wood, paper and other forest products sourced from well-managed forests continues to grow. Consumers and business partners want assurance that your products come from responsibly managed sources that limit their damage to the forest environment and forest-dependent indigenous communities.

Your business must also prove that your goods come exclusively from legal sources as required by the EU Timber Regulation, the Lacey Act in the U.S., or similar legislative requirements. WHAT IS FSC™ CHAIN OF CUSTODY CERTIFICATION? The Forest Stewardship Council™ (FSC) is a nonprofit organisation that set standards for forestry practices with the aim of promoting environmentally responsible and socially beneficial forestry. Wood products such as furniture can be labelled as FSC certified if they meet the high standards set by the organisation. To be certified, the flow of the wood material – from the forest to the customer – must be monitored to demonstrate its origins. This evidence is known as Chain of Custody (CoC).

WHY IS IT IMPORTANT? This assures customers that your company only uses legal sources and responsibly managed forests for its material. It enables you to offer your customers better value in terms of origin of material and promotion of responsible forestry. By using FSC™ material, you can also open up new business opportunities for your company in markets requiring the certification. OUR FSC™ COC SERVICES We offer services to support your company at every stage of the certification process, from pre-audit throughout the entire five-year certification cycle. SHOW YOUR COMMITMENT TO PROTECT OTHERS AND THE ENVIRONMENT With increasing global focus on commerce and industries’ sustainability efforts, the onus is on businesses to produce environmentally-friendly products.

This is particularly the case for the electronics industry where the current production processes of most electronic and electrical products include use of hazardous substances. Regardless of whether these hazardous substances are essential to the functionality of a product or a result of the manufacturing process, the presence of such substances cannot be ignored. WHAT IS IECQ QC 080000? The IECQ QC 080000 Hazardous Substance Process Management (HSPM) system is based on the international quality management system ISO 9001. It covers the key requirements of the various environmental protection directives such as the Restriction of use of certain Hazardous Substances in Electrical and Electronic Equipment (RoHS) and Waste Electrical and Electronic Equipment (WEEE). The IECQ QC 080000 system seeks to minimise or eliminate the production of the hazardous substances to demonstrate to your customers, employees and shareholders that your organisation is committed to ensuring the sustainability of...

The system is structured to complement any existing management systems in place such as ISO 9001. WHY IS IT IMPORTANT? Most current manufacturing and production processes are thoroughly examined and evaluated for their use and production of hazardous substances specified for special restriction. With the IECQ QC 080000 certification, not only do you receive a guideline for your business’ path ahead, you commit to ensuring the safety of all staff involved. This includes those on the assembly line, users of your product, and individuals potentially affected through its impact on the environment.

About Us In South Asia Tüv Süd In India

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