Featured Testimonials
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.
Sr. Manager, Regulatory Affairs – Labeling and AdPromo
UK-based, Multinational Pharmaceutical and Biotechnology Company
Medicinal Products
Promotional review
USA
Our AdPromo review relationship with Freyr is continuing to evolve as we move forward. The team is collaborative and responsive. We are happy to collaborate with you on this important program.
Business Development Team, FDF RoW market
India-based, Multinational Pharmaceutical and Biotechnology Company
Medicinal Products
Conference Support
India
I wanted to thank you and all the team who have worked on this project around the clock. You and your team exhibited good time management and customer service skills throughout the project by promptly responding to our queries and accommodating multiple iterations of the design and content. all of this has led the project to be delivered within such short deadlines.
Thank you once again and we look forward to working with you again when the opportunity presents itself.
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.
Director - Global Regulatory Affairs – Operations
India-based, Global Top Generic Pharma Company
Medicinal Products
Regulatory Affairs
India
Thank you for the timely support over the weekend, which allowed us to resubmit quickly after being notified. This continuously demonstrates Freyr's commitment towards our company’s milestones.
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.
Sr. Director, Head of Regulatory Operations
Ireland-based, Global Specialty Pharmaceutical Company
Medicinal Products
Publishing
UK
I am sure you have heard by now that we have received our first-ever approval from the FDA for our Brands division. This is a major milestone for us as well as for my team here in Reg Ops. I would be remiss if I didn’t point out that we would not have been able to do this without the help of your dedicated team. From the original filing, then the following year of responses, all helped get us to final approval.
Thank you Freyr team for a job well done!
Head of Quality Assurance
Medicinal Products
Medical Writing
India
A big thanks to Freyr team for the support they have provided to us on priority. We really appreciate the extra effort that the Freyr team has put into providing the reports on time. We are looking forward for a continuous business association with Freyr.
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.