April 30, 2020

The Government of Hong Kong issued an updated list of standards for toys and children products. According to the Decree (cap 424) manufacturers of the following classes of products must meet the relevant requirements of the applicable safety standards to put the produc...

April 29, 2020

New lists of harmonized standards was published in the Official Journal of the EU on March 25, 2020. 

The lists relate to the three Directives on medical devices: 

  • Council Directive 93/42/EEC of June 14, 1993 concerning medical devices

  • Council Directive 90/...

April 24, 2020

In China, a new category of standard for donated textiles appeared. The new standard GB/T 38418-2019 “General Technical Requirements for Donated Textiles” specifies terms and definitions of donated textiles, product classification, technical requirements, test method,...

April 23, 2020

ONTARIO REGULATION 30/20 on Batteries under the Resource Recovery and Circular Economy Act, 2016 was published in The Ontario Gazette on March 14, 2020.

This Regulation applies to primary and rechargeable batteries with a weight of 5 kg or less. The document establishes...

April 21, 2020

Entering a new market is a real challenge especially for manufacturers of telecom products whose industry is specific and highly competitive. Moreover, many accessories and components of such equipment may have special terms within the market access procedure.

Learn how...

April 20, 2020

The Saudi Standards, Metrology, and Quality Organization announced that it will extend certificates of conformity if they were registered on the Saber platform and their validity period ends in March, April or May 2020. Such certificates will be valid for three months...

April 16, 2020

The Government of South Korea keeps paying attention to the process of saving and recycling of resources. Recently, it launched the evaluation system to control the quality and structure of packaging materials. According to this system, manufacturers of recyclable pack...

April 10, 2020

Due to the coronavirus epidemic and preventative measures taken in Russia, Federal Security Service (FSS) introduced limitations on personal submission and issuance of original documents. Until the end of April,  documents can be submitted only by postal services. If t...

April 1, 2020

All medical devices to be placed on the EU market must have a CE mark. Thus, a medical device must meet requirements of the EU ruling documents. The Directives 90/385/EEC and 93/42/EEC were used previously. However, EU MDR was established in 2017 and preliminary should...

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Do not hesitate to contact us for more information.

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