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<\/span><\/li><\/ul><\/div><\/div><\/div><\/div><\/div><\/div>Service Regulation in Uruguay<\/h2>\n
Manufacturers of medical devices that wish to distribute and market their products in Uruguay must comply with Uruguayan legislation, that is, for a medical device to enter the country, it must obtain the health registration issued by the country’s health authority (Ministry of Public Health – M.S.P.).<\/p>\n
Passarini Group<\/strong>, through its technical team in Uruguay,<\/a> offers the comprehensive advice and support you need to comply with the regulatory framework in all its stages.<\/p>\n<\/div>
Discover some of the services we provide in Uruguay:<\/h2>\n<\/div>
<\/i><\/i><\/span>Product Registration<\/span><\/a><\/h4><\/div>
\nWe register the following products: Cosmetics, Medicines, Therapeutic Devices, Diagnostic Reagents, Medical Equipment, Domestic Sanitary Products, Modified Foods and Dietary Supplements. All before the Ministry of Public Health of Uruguay.<\/p>\n<\/div><\/div><\/div>
<\/i><\/i><\/span>Creation or Modification of Regulations<\/span><\/a><\/h4><\/div>
\nWe work together with our legal advisors or the contracting company in generating proposals for the creation or modification of regulations.<\/p>\n
We generate alerts to our clients in the face of regulatory changes that may impact their operations.<\/p>\n
We prepare reports on regulations under public consultation or recently enacted.<\/p>\n<\/div><\/div><\/div>
<\/i><\/i><\/span>Registration Maintenance\/Hosting<\/span><\/a><\/h4><\/div>
\nOur company is in a position to immediately register and be the owner and importer of the following types of products:<\/p>\n
- \n
- Foods<\/li>\n
- Cosmetics and related<\/li>\n
- Sanitizers for domestic use<\/li>\n
- Therapeutic devices<\/li>\n
- Diagnostic reagents<\/li>\n<\/ul>\n<\/div><\/div><\/div>
<\/i><\/i><\/span>Technical Direction<\/span><\/a><\/h4><\/div>
\nA professional from our company can perform Technical Management with the support of our professional and technical team.<\/p>\n
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- Implementation and coordination of the quality assurance system.<\/li>\n
- Leadership of the recall process and associated decisions where appropriate.<\/li>\n
- Supervising\/performing internal audits or self-inspections.<\/li>\n
- Maintenance of company authorizations before the health authority.<\/li>\n
- Attention to technical questions.<\/li>\n
- Supervision of the product destruction process.<\/li>\n<\/ul>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>
See below our complete MSP process flow<\/h2>\n<\/div>
![](\"https:\/\/passarini.com.br\/wp-content\/uploads\/2022\/12\/Fluxo_Etapas_EN_Process_Uruguay_MSP_LATAM-300x181.webp\")
<\/a><\/div><\/div><\/div>Passarini Group<\/strong> is a company that has the best specialists in Regulatory Consultancy of Medical Products, applying the One Stop Shop<\/strong> concept daily in your company with practical solutions.<\/p>\n<\/div>