Verified email-pattern data for Practical Ra is currently limited. You can still use the company insights and contact sections below.
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
- -
- Address
- London, Gb
- Industry
- Medical Equipment Manufacturing
- 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
Global Certification Body (Gcb),
Dellbrook | Jks,
Princesse Parfums.
Practical RA's categories are Medical Equipment Manufacturing
Practical RA's founding year is 2019
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