WHO WE ARE
SGR is an expert mexican company in providing solutions in Health Regulation for companies dedicated to the marketing of Health Supplies, Technovigilance and Sanitary Registers of Medical Devices.
We provide a complete managment to achieve your objectives, being your regulatory partner by reviewing all characteristics of your products in detail, such as approvals and legal documents you might have.

Vision
SGR-Especializada wants to become a renowned regulatory company by providing the best and greatest service and support to our customers throughout the entire process of their product’s lifecycle, in compliance with current regulations and helping new medical technologies be available to Mexicans through medical devices.
Mission
SGR-Especializada analyses, provides support and contributes to implement regulatory strategies to develop and establish integrated solutions for the entry into the national and international market of health care products.

Vision
SGR-Especializada wants to become a renowned regulatory company by providing the best and greatest service and support to our customers throughout the entire process of their product’s lifecycle, in compliance with current regulations and helping new medical technologies be available to Mexicans through medical devices.

Mission
SGR-Especializada analyses, provides support and contributes to implement regulatory strategies to develop and establish integrated solutions for the entry into the national and international market of health care products.

SERVICES
Sanitary Register of Medical Devices, class I, II and III
Renewal of Sanitary Registrations of Medical Devices, class I, II and III
Operation Notice and Health Responsible Notification
Advertising notices for health professionals.
Registration of the Technovigilance Resposible and Technovigilance Manager
Sanitary Import Permit for Medical Devices
We are a pioneer company in the development of regulatory solutions, we are a consultancy that understands the necessary documentary requirements, the processes, being experts in the establishment of Quality Management systems that in turn allow the creation of regulatory files to obtain Sanitary Registrations from the most consolidated worldwide to the most innovative developments in all categories of Medical Devices.
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