We offer comprehensive tools and training in regulatory affairs for medical devices.
Our online training courses are written and presented by regulatory experts and cover practical, up-to-date information on EU and US medical device regulations.
In 2024, we launched our SAGE AI EU MDR submission builder, designed specifically for small businesses to compile a robust, compliant EU medical device submission through an intuative, step-by-step process.
Whether you’re looking to get your first product approved or streamline your compliance processes, our offerings are designed with your success in mind.
Company Details
- Founded
- 2019
- Address
- London, Gb
- Industry
- Medical Equipment Manufacturing
- NAICS
-
Medical Equipment and Supplies ManufacturingSurgical and Medical Instrument ManufacturingSurgical Appliance and Supplies ManufacturingDental Equipment and Supplies ManufacturingOphthalmic Goods ManufacturingDental Laboratories
- Website
- https://www.practicalra.com/
- Keywords
- EU MDR, US FDA, Risk Management, Clinical Evaluation Reports, Post-Market Surveillance, Quality Management Systems, Online training, Quality Assurance, Consulting, Medical Devices, Regulatory Affairs, Australian TGA, Market Access.
- HQ
- London
Practical Ra Questions
Practical Ra's website is https://www.practicalra.com/
Practical Ra's LinkedIn profile is https://uk.linkedin.com/company/practical-ra
Practical Ra's industry is
Medical Equipment Manufacturing
Practical Ra's top competitors are
Dellbrook | Jks,
Princesse Parfums,
Global Certification Body (Gcb).
Practical Ra's categories are Medical Equipment Manufacturing
Practical Ra's founding year is 2019
