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  • Indonesia SDPPI Guide for R&...

    Indonesia SDPPI Guide for R&TTE Device -> REGULATORY AGENCY Directorate General of Posts and Informatics Resources (SDPPI) REGULATIONS Certification by type approval of regulated products is required. Product testing should be performed by an in-co

  • India CDSCO Guide for Medica...

    India CDSCO Guide for Medical Device -> REGULATORY AGENCY Central Drugs Standard Control Organisation (CDSCO, Directorate General of Health Services, Ministry of Health and Family Welfare, Government of India REGULATIONS Some medical devices are regu

  • India BEE Guide for Environm...

    India BEE Guide for Environmental -> REGULATORY AGENCY Bureau of Energy Efficiency (BEE), Ministry of Power REGULATIONS ENERGY EFFICIENCY The mandatory energy efficiency Star Label is required for certain products under the Standards & Labelling Pro

  • India ISI Guide for Safety D...

    India ISI Guide for Safety Device -> REGULATORY AGENCY Bureau of Indian Standards (BIS) REGULATIONS The ISI Mark or Standard Mark, is issued by BIS under its certification scheme. ISI certification* is a self-regulation scheme.

  • India CRS Guide for Safety D...

    India CRS Guide for Safety Device -> REGULATORY AGENCY Department of Electronics and Information Technology (DietY) REGULATIONS The Compulsory Registration Scheme (CRS) covers 30 types of electronics and information technology goods.

  • India TEC Guide for Telecom ...

    India TEC Guide for Telecom Device -> REGULATORY AGENCY Telecommunication Engineering Centre (TEC), Department of Telecommunications REGULATIONS Type approval is required to indicate compliance with Generic Requirements (GR).

  • India WPC Guide for Wireless...

    India WPC Guide for Wireless Device -> REGULATORY AGENCY Wireless Planning and Coordination Wing (WPC), Ministry of Communications and IT, Department of Telecommunications

  • Malaysia MDB Guide for Medic...

    Malaysia MDB Guide for Medical Device -> REGULATORY AGENCY Medical Devices Bureau (MDB), Ministry of Health REGULATIONS All medical devices to be placed in Malaysian market are required to be registered under Act 737. It is a mandatory requirement

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