Client Testimonials
  • Regulatory Affairs Manager​
    US-based, Leading Pharmaceutical-grade Chemicals Manufacturing Company

    Pharmaceuticals

    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

    Pharmaceuticals

    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​

    Pharmaceuticals

    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

    Pharmaceuticals

    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​

    Pharmaceuticals

    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

    Pharmaceuticals

    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​

    Pharmaceuticals

    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

    Pharmaceuticals

    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.​

  • Key Accounts Manager​
    China-based, Leading Medical Device Manufacturing Company​

    Medical Devices

    Device​ Registration​ and LR services​

    Thailand

    We appreciate the efforts and expertise of the Freyr team during the registration procedure. The accomplishment is ahead of schedule, which is really wonderful. Cost-effective and the service is nice. A timely response is to your advantage. Hope we can work together on other projects. ​

  • Managing Director​
    India-based, Leading Global Medical-Technology Company​

    Medical Devices

    Device Registration

    India

    A good product is developed not only by a technology, but with the real science and its validation to the norms of regulations. We couldn’t have achieved it without your able guidance and experience. ​