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Untangling the Regulations of Health Tech Blog Pure Global

WebDigital Health Technology Landscape. The digital health technology landscape is heavily skewed towards health and wellness applications. Typical examples include apps to …

Actived: 9 days ago

URL: https://www.pureglobal.com/blog-posts/untangling-the-regulations-of-health-tech

Your Gateway to North America's Growing Healthcare Market

WebCanada. Your Gateway to North America's Growing Healthcare Market. Canada, with its population of over 38 million, relies heavily on imports to meet approximately 70% of its …

Category: Health Go Health

ANVISA Brazil Medical Device Registration Pure Global

WebBrazil, the heart of Latin America, boasts a population of 214 million and ranks as the eighth largest healthcare market globally. With around 50% of medical devices and IVDs …

Category: Medical Go Health

We Provide Access To Markets Worldwide Pure Global

WebTailored Support for Market Entry. Partner with us to streamline your market access and regulatory compliance efforts, minimizing the risk of application rejections and reducing …

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ANVISA's Collegiate Board Meeting Opens to Public Participation

WebOn March 6, 2024, ANVISA held DICOL, which are meetings of the Collegiate Board (Dicol) of the National Health Surveillance Agency (Anvisa) that occur periodically and are open …

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Simplifying Medical Device Regulation Compliance Pure Global

WebThe Medical Device Division (MDD) oversees the Medical Device Administrative Control System (MDACS), facilitating a pathway towards establishing a statutory regulatory …

Category: Medical Go Health

AMAR Israel Medical Device Registration Pure Global

WebIsrael, with its advanced healthcare sector and a strong focus on technological innovation, presents a dynamic market for medical devices. The country's regulatory environment is …

Category: Medical Go Health

Simplifying Medical Device Registration for Vietnam's Growing …

WebThe Department of Medical Equipment and Construction (DMEC) within the Ministry of Health (MOH) oversees the registration and licensing of Class B, C, and D medical …

Category: Medical Go Health

Simplifying Medical Device Registration with DIGEMID Pure Global

WebIn Peru, the General Directorate of Drugs, Supplies and Drugs (DIGEMID) oversees the registration and regulation of medical devices. A sanitary registration is mandatory for …

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Navigating the UK's Medical Device Regulatory Landscape

WebUnited Kingdom. Navigating the UK's Medical Device Regulatory Landscape. With a population nearing 68 million and ranking as the third-largest medical device market in …

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Unlocking the Potential of Bangladesh's Growing Healthcare …

WebThe Directorate General of Drug Administration (DGDA), under the Ministry of Health and Family Welfare, is the regulatory authority overseeing the registration, importation, and …

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Connect With Us At MedTech Events Pure Global

WebRAPS Euro Convergence is the most comprehensive regulatory affairs conference in Europe, focusing on the latest developments in healthcare products in Europe and …

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EDA Egypt Medical Device Registration Pure Global

WebEgypt follows device classification guidelines similar to reference markets such as the CE (European Conformity), US FDA, and Health Canada. Class I non-sterile devices are …

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Pure Global COO Joins Elite Panel: China-Brazil Bio Forum

WebPure Global COO, DJ Fang, Engages in Key Talks at AstraZeneca's China-Brazil Biomedical Forum to discuss medical innovation.

Category: Medical Go Health

Brazilian Markets Navigation: Pure Global Alliance Blog Pure …

WebANVISA's Role in Regulation. Brazil is the largest medical device market in Latin America. The Brazilian regulatory registry for medical devices and in-vitro diagnosis is managed …

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MOHAP UAE Medical Device Registration Pure Global

WebThe United Arab Emirates, with its strategic location and robust healthcare infrastructure, is a burgeoning market for medical devices. The country's commitment to healthcare …

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NMPA China Medical Device Registration Pure Global

WebThe National Medical Product Administration (NMPA) is the regulatory body overseeing medical devices in China. All medical devices must be registered with the NMPA before …

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Our Blog Pure Global

WebLet's Talk, Anywhere You Are. Whether looking for more information or ready to partner with us, we're here to guide you through every step of the regulatory process. Our closest …

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