Featured Testimonials
Tygrus LLC

Tygrus LLC (AMR)

Chemicals

USA

 

Expanding globally was complex until we partnered with Freyr. Their deep Regulatory knowledge and prompt support helped us register products efficiently across regions. From chemical imports to fertilizer compliance, their solutions were spot-on. Freyr’s professionalism, quick turnarounds, and high-quality service exceeded expectations. We highly recommend Freyr to any business seeking expert Regulatory guidance.

Swiss PharmaCan AG (Europe, US, Asia)

Swiss PharmaCan AG

Food Supplements

Europe, USA

 

Partnering with Freyr for Regulatory compliance in the Indian market proved a strategic decision. Their team demonstrated a high level of professionalism, Regulatory expertise, and responsiveness throughout the engagement. Freyr consistently delivered timely solutions, ensuring clarity and confidence at every project stage. Their continued support, even post-completion, reflects a strong commitment to client success. We confidently recommend Freyr as a trusted partner for navigating complex Regulatory frameworks.

Vush

Vush

Food Supplements

Australia

 

Freyr has been an exceptional partner in streamlining our multi-region Regulatory compliance. Their ability to act as a single point of contact and structured tracking systems has simplified complex processes and reduced our workload. From compliance gap analysis to product registration and representation, their execution is precise and timely. What truly stands out is their responsiveness, clarity, and deep Regulatory expertise. I highly recommend Freyr for its reliability, efficiency, and commitment to Regulatory excellence

Owen Mumford Ltd (Europe, US, Asia)

Owen Mumford Ltd

Food Supplements

Europe, USA

 

Freyr has been an invaluable partner in navigating complex Regulatory landscapes. Their professionalism, responsiveness, and deep expertise ensured smooth execution, even in challenging markets like Japan. We highly recommend Freyr for its commitment to quality and reliable Regulatory support.

  • System Owner​

    UK-based, Multinational Pharmaceutical and Biotechnology Company​

    Medicinal Products

    Regulatory Affairs

    UK

     

    Thank you, Freyr, for all your help with the informal testing, constructive feedback, and positive engagement. ​

  • Regulatory Consultant​

    US-based, Leading Pharmaceuticals Manufacturing Company​

    Medicinal Products

    Regulatory Affairs

    USA

     

    Please relate to the team the excellent job they have done on the IND reactivation. Specifically, the high-quality module 3, written by Freyr. It was very comprehensive, very few revisions were required, and we had no questions from Health Canada or FDA. No CMC questions; that was a first for me. So very responsive to my many requests, which I am sure can be frustrating but always helpful while producing excellent work. ​

    Thank you for always being available and responding quickly and comprehensively to all my requests.

    What a great team you have, Freyr.

  • Regulatory Affairs Manager​

    US-based, Leading Pharmaceutical-grade Chemicals Manufacturing Company

    Medicinal Products

    Regulatory Affairs

    USA

     

    I honestly can't think of any suggestions for improvement at Freyr's end. As I've said before, Freyr is terrific to work with, more so than any other consultant I've dealt with. Freyr's team was all incredibly responsive, helpful and met every timeline as they stated originally. I was very impressed with the team's professionalism and kindness. I mean it when I say I hope to work with Freyr on additional projects. I'll be reaching out to the team soon with details of future projects. ​

    Thank you, everyone at Freyr, for your excellent efforts – it is sincerely appreciated!

  • Vice President R&D​

    Canada-based, Leading OTC Products Company

    Medicinal Products

    Regulatory Affairs

    Canada

     

    Thanks for sending the invoice. The activities and amounts generally mesh with our expectations. The provided resource is doing a great job managing our projects and keeping us informed of the status. We are very happy with her diligence, professionalism, and high level of service. For tracking these types of hourly activities in our internal records, it would be helpful if you could provide a summary of the hours by month or by country if that is possible.​

  • Assistant Manager | Global Regulatory Affairs​

    South Korea-based, Global Biopharmaceutical Company​

    Medicinal Products

    Regulatory Affairs

    South Korea

     

    Completing the CTD writing project with Freyr was really helpful and cooperative. Thank you very much for your support and effort. Freyr Solutions very well understand the 'Asian culture'; sometimes, we ask for completing the project in stringent timelines, but Freyr accepts this kind of urgent request and completes them on time. ​

  • Vice President - Regulatory Affairs​

    India-based, Fast-growing Pharmaceutical Company

    Medicinal Products

    Regulatory Affairs

    India

     

    I would like to let you know that we are happy with your services. The team did a good job, both qualitatively and quantitatively.​

  • Director RA​

    US-based, Leading Generic Pharmaceutical Company​

    Medicinal Products

    Regulatory Affairs

    USA

     

    I just wanted to say how pleased we are with your resource's work. He has quickly come up to speed and is doing a great job.​

    Thank you for listening to our needs and finding such a great match.​

  • Regulatory Affairs (Formulation R&D)

    US-based, CRO Company that Focuses on Material Science and Engineering for Drug Development

    Medicinal Products

    Regulatory Affairs

    USA

     

    Thanks a lot for your extended support at the last moment. We really appreciate your amazing dedication and efforts.​

  • CEO

    US-based, CRO Company that Focuses on Material Science and Engineering for Drug Development​

    Medicinal Products

    Regulatory Affairs

    USA

     

    Many thanks for your efforts, especially at the last minute.​

  • SVP - R&D ( Finished Dosage Form)​

    US-based, CRO Company that Focuses on Material Science and Engineering for Drug Development

    Medicinal Products

    Regulatory Affairs

    USA

     

    Kudos to you all for the brilliant teamwork!!! Alone, we can do so little; together, we can do so much. Look forward to the next milestone and collaboration on new projects in the future.​