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Mundomedis and Arazy Group Sign Cooperation MoU

Mundomedis and Arazy Group Sign Cooperation MoU

by arazygroup | Jan 5, 2022 | Blog, Top Story Slider

By Mundomedis | 7th December 2021 Mundomedis FZCO and Arazy Group recently signed a cooperation memorandum. Both companies will cooperate to support Mundomedis’ global medical device portfolio companies by streamlining their global regulatory processes through...
Certain Medical Devices in India will be Considered as Drugs as of 30 June 2022

Certain Medical Devices in India will be Considered as Drugs as of 30 June 2022

by arazygroup | Nov 22, 2021 | Blog, Top Story Slider

By Fajar Dumadi | November 23, 2021 On February 8, 2019, the Ministry of Health & Family Welfare, Government of India, has notified that the following devices were regulated as drugs; effective from April 1, 2021: All implantable medical devices CT scan equipment...
Medical Device Registration and Supply in Ukraine

Medical Device Registration and Supply in Ukraine

by arazygroup | Mar 11, 2022 | Blog, Regulatory News Slider, Top Story Slider

By Fajar Dumadi | March 11, 2022 In regards to the enforcement of martial law on February 24th, 2022, the Ministry of Health allows the supply of medical devices, in-vitro diagnostics, and implantable medical devices that do not comply with the requirements of the...
Medical Devices Registration Exemption in Pakistan

Medical Devices Registration Exemption in Pakistan

by arazygroup | Oct 28, 2021 | Blog, Regulatory News Slider, Top Story Slider

By Fajar Dumadi | October 20, 2021According to the Medical Device Rules 2017, “A medical device that is essential to or that yields information that is essential to the restoration or continuation of a body function important to the continuation of human or...
Mandatory Registration Scheme for Non-Notified Medical Device in India

Mandatory Registration Scheme for Non-Notified Medical Device in India

by arazygroup | Oct 1, 2021 | Blog, Regulatory News, Top Story Slider

By Fajar Dumadi | October 20, 2021 Non-notified medical devices were non regulated products; therefore, registration certificate was not required. According to the Medical Device (Amendment) Rules – February 2020 (1), which was enforced in April 2020, all...

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    Arazy Group Consultants Inc. is an international consultancy spanning several continents, assisting medical and IVD device companies with regulatory compliance and affairs as they try to enter new markets

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