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Following consultation with stakeholders, India’s Drugs Controller General adopted essential principles for safety and performance of medical devices marketed in India. Read More
Following up on a proposal from Australia’s Therapeutic Goods Administration, the International Medical Device Regulators Forum released a new consultation on personalized medical devices following its March meeting in Shanghai. Read More
The International Medical Device Regulators Forum released updates from its working groups on good regulatory review practices, unique device identifier harmonization, adverse event terminology and standards. Read More