Capitalise on international opportunities by accessing global markets
Manufacturers, importers, retailers or traders seeking to bring their electrical and electronic products to the global market face challenges in managing compliance with technical regulations. In the absence of harmonised standards and requirements as well as differing national standards across countries and regions, manufacturers need to be aware of the regulations for each country or region they want to access. Some countries and jurisdictions impose specific technical restrictions such as product testing, certification and shipment inspection requirements. In addition, the complex regulatory framework in some countries is constantly being updated and expanded.
Global Market Access (GMA) is the process of determining applicable regulations and managing product compliance to those regulations with respect to accessing global markets.
Bringing electrical and electronic products to market in different countries is complicated. Non-compliant products must be redesigned or reengineered, resulting in delays and loss of revenue. Customs officials may impound or deny access to non-compliant products, exposing manufacturers to potential legal consequences.
We act as your international regulatory approvals department. Our experts provide guidance on the compliance requirements and approval strategy for each country. We also perform product testing to the correct test standards as required, in some cases provide access to local representation for clients with no presence in the respective countries or regions, prepare applications on your behalf, perform a post-submission follow-up with the authorities/ certification bodies, conduct training for your staff on technical standards used for implementation of regulations, and update you on the latest regulatory changes.
Our GMA services cover additional product categories that are not listed in the above. Click here to find out more Global Market Access services related to Automotive components and Healthcare and Medical Devices.
As a globally renowned solutions provider, TÜV SÜD has strong working relationships with regulators and national certification bodies in key markets. We are designated as a Conformity Assessment Body through Mutual Recognition Agreements (MRA) with various regulators across the globe for issuing test reports/Certificate of Approval for products sold to the countries of MRA partners. We act as a Notified Body for various European Directives and are authorised by OSHA as a Nationally Recognized testing Laboratory (NRTL) in America. We participate actively in the international Conformity Assessment arena, such as the IECEE CB Scheme, where we are among the top issuers of certificates for the product categories. Our GMA service is accessible to you worldwide through our team of dedicated GMA managers who are able to work and converse in your language.
Please note that our service scope is not limited to the listed countries / regions and products.
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