Featured Testimonials
Bien Almonte
QC & Regulatory Manager
Food Supplements
Freyr exceeded our expectations by delivering a hassle-free and smooth product registration experience in the EU. Their team was professional, responsive, and always ready to provide clarity when needed. As a result, we are now confidently operating in five EU countries with our dietary supplements, thanks to their expert guidance and flawless execution. We highly recommend Freyr for regulatory support.
KASIA FRANKOWSKA
Head of Regulatory Affairs
Cosmetics
End-to-end regulatory services
Global
It has been a pleasure working with Freyr, thanks to the seamless project delivery and the value your team consistently brought to the table. The expertise and professionalism demonstrated have exceeded expectations. I look forward to future opportunities to collaborate.
Arie Henkin
VP - Quality and Regulatory, Australia -based, Leading SaMD Company
Medical Devices
Registration and LR Support
Global
Freyr has been an indispensable partner in achieving rapid global scalability for our Software as a Medical Device (SaMD) business. As a startup, acquiring expertise in worldwide regulations is cost-prohibitive. Freyr's competitive pricing and tailored services allowed us to get that expertise at a fraction of the cost of full-time resources. Their team's responsiveness and adaptability to project priorities have greatly facilitated our progress. We recommend Freyr to any company seeking expert guidance and support in the medical device Regulatory domain.
Ed Venkat
Global CMC Technical Lead
Medicinal Products
Publishing and Submission
UK
We would like to appreciate Freyr’s quick TAT to push through an urgent submission required by the FDA. Their efficiency, diligence, excellence, sense of urgency, and priority are deeply flexibility.
Please keep up the great work as we have many milestones to achieve over the next year.
Bill Birdsall
Chief Compliance Officer
Medical Devices
Registration and LR Services
Global
Many, many thanks to the amazing team at Freyr Solutions for all your efforts and tireless support, making us the world leader in AI-driven dental solutions. We are grateful for all you have done and continue to do
Regulatory Affairs Officer
UK-based, global Medical Device Manufacturing company
Medical Devices
Device Registration
UK
You have exceeded our expectations as a team and individuals! Special thanks for all the added prepared technical documentation!! What an effort, team! Again, many thanks for all the work and efforts put into this, moving forward positively.
Lead - Regulatory Affairs
Lead - Regulatory Affairs, Russian Medical Device Manufacturer
Medical Devices
Registration and LR services
Global
Freyr has been our reliable Regulatory partner and possesses deep understanding of the technical documents. Freyr has provided us timely support for gap analysis which led to timely registration. We are highly impressed with the customer support we received from Freyr in understanding our queries and providing us timely and accurate resolution.
Arie Henkin
VP - Quality and Regulatory, Australia -based, Leading SaMD Company
Medical Devices
Registration and LR Support
Global
Freyr has been an indispensable partner in achieving rapid global scalability for our Software as a Medical Device (SaMD) business. As a startup, acquiring expertise in worldwide regulations is cost-prohibitive. Freyr's competitive pricing and tailored services allowed us to get that expertise at a fraction of the cost of full-time resources. Their team's responsiveness and adaptability to project priorities have greatly facilitated our progress. We recommend Freyr to any company seeking expert guidance and support in the medical device Regulatory domain.
Darren Mansell
Regulatory Affairs Manager, UK-based, Global Medical Device Design and Manufacturing Company
Medical Devices
Swiss Rep Services
Japan and Switzerland
I genuinely enjoy my time working with Freyr, and I view them as a truly valuable asset and extension to my own team. They are dependable and accurate, and their pricing is competitive. Beyond that, I won’t hesitate to collaborate with Freyr again.
Robert Menadue
Regulatory and Quality Assurance Manager, Australia-based, Medical Device Manufacturing and Distribution Company
Medical Devices
Registration and AR Services
Malaysia and Indonesia
Freyr provides a reliable service with expertise across many countries. I can rely upon Freyr to provide the information necessary to make an informed decision before entering a formal scope of work agreement. Once a project is underway, the Freyr team acts professionally to execute the work with excellent communication of progress.
Sergey Burlov
Quality Manager, Russia-based, Innovative SaMD Company
Medical Devices
Registration and LR Services
Brazil
We are impressed with Freyr’s support in providing us with quick and well-detailed solutions to our queries. Freyr’s constant support to adapt to ever-changing Regulatory conditions while providing support with any additional queries we had in a timely manner has truly impressed us.
Pascale LE BAUD
Regulatory Affairs Associate - RA Department, France-based, Leading Synthetic Implants Manufacturing Company
Medical Devices
UKRP Support
UK
FREYR has accompanied us with the registration of several products on the UK market. They have always been quick to reply, attentive to our needs, a great source of Regulatory information and support. The price is reasonable compared with other similar service providers. We particularly appreciate the personalized quarterly and annual status reports that Freyr provides. When we call on FREYR, we know they will do their best to satisfy our needs, and that customer satisfaction is a priority.
Regulatory Affairs Officer
UK based, global Medical Device Manufacturing company
Medical Devices
Technical Documentation
UK
You have exceeded our expectations as a team and as individuals! Special thanks for all the added prepared technical documentation!! What an effort, team! Again, many thanks for all the work and efforts put into this, moving forward positively.
Regulatory and Quality Assurance Manager
Regulatory and Quality Assurance Manager
Medical Devices
Registration and AR Services
Australia
Freyr provides a very reliable service with expertise across many countries. I can rely upon Freyr to provide the information necessary to make an informed decision before entering a formal scope of work agreement. Once a project is underway, the Freyr team act professionally to execute the work with excellent communication of progress