Capitalise on the market opportunities in India
Regulations and compliance requirements can pose challenges to companies who are exploring new markets overseas. Most products entering the Indian market must meet the relevant requirements of the authorities depending on the product scope. These product safety requirements and regulations are put in place to reduce risks, improve quality of life and ensure safety during use.
You can ensure that your products successfully meet the Indian standards by working with a market leader, TÜV SÜD. TÜV SÜD fully understands the local requirements and procedures applicable in India. You can rely on our expertise and knowledge to help you access key markets efficiently while at the same time, be assured of our objectivity, integrity and professionalism.
* Certification procedure and submission requirements differ between foreign manufacturers and Indian importers.
** The simplified procedure is not granted to some items under mandatory certification and all first-time licenses for any product.
A full list of product categories may be found here. To determine if a particular product is subject to the above regulations, please contact us.
To determine if a particular product is subject to the above regulations, please contact us.
* Under Schedule M-III, the proposed regulation follows the same structure as the EU Medical Device Directive 93/42/EEC. Device classifications A, B, C and D are harmonised with the Global Harmonisation Task Force. The proposed requirements are summarised as follows:
* TEC issues certification of approval in particular cases, specifically for GSM phones, 3G modems, Bluetooth-enabled wireless terminals against approved Standards of Standard Body.
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