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Sanrubio LLC, provides specialized regulatory consulting for medical devices, guiding companies through the FDA regulatory process in the United States. Our services encompass preparation and submission of 510(k), De Novo, and Pre-Submission filings. Additionally, we offer expert consulting to ensure compliance with international standards such as ISO 13485, MDSAP, and 21 CFR 820.
In an industry where quality and safety are paramount, our multidisciplinary team is equipped to design tailored strategies that deliver value and build trust.
Company Details
- Employees
- 1
- Founded
- -
- Address
- Miami, Florida 33126, Us
- Industry
- Professional Services
- Website
- http://mdevicesconsulting.com/en
- Keywords
- Medical Device Regulatory Consulting, FDA Regulation (510(k), De Novo, Pre-Submission), 21 CFR 820 & Good Manufacturing Practices, Market Entry Strategies for Medical Devices, Medical Device Quality Management, Regulatory Audits & Assessments, Consultoría regulatoria para Dispositivos Médicos, ISO 13485, MDSAP, Buenas prácticas de manufactura.
- HQ
- MIAMI, Florida
Sanrubio, Llc Questions
Sanrubio, LLC's website is http://mdevicesconsulting.com/en
Sanrubio, LLC's LinkedIn profile is https://www.linkedin.com/company/sanrubio
Sanrubio, LLC has
1 employees.
View email and phone details for 1
employees at Sanrubio, LLC.
Sanrubio, LLC's industry is
Professional Services
Sanrubio, LLC's top competitors are
510k Guru,
Ruta Al Empleo,
Imta,
Centro Regional De Seguridad Hídrica Bajo Los Auspicios De Unesco,
Th Asesores,
Fda - Medical Devices,
Indautor,
Red Del Agua Unam,
Ap Resolve Capacitación Y Validación Para La Industria Farmacéutica, Dispositivos Médicos Y Salud,
Newclip Iberia.
Sanrubio, LLC's categories are Professional Services
Sanrubio, LLC's founding year is 2021
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JOSE HUERTA
Director En Sanrubio, Llc
Miami, Florida, United States, United States1exo.com.ar
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