Featured Testimonials
Poonam Dharman

Packaging and Artwork Director, Lipton Teas and Infusions

Food Supplements

Netherlands

 

Working with Freyr has lifted some of the worries and burden of complying with intricate packaging regulations and the ever changing requirements and landscape. We now know that we are in safe hands as we continue working with them. If you are a company who also gets baffled on understanding complicated packaging compliance requirements, then I highly recommend Freyr as a reliable and valuable partner for packaging regulatory projects.

Cana Eisenhaur

Regulatory and Quality Manager, Bluu GmbH

Food Supplements

Germany

 

My experience with Freyr was great. The team was always there when needed. Deadlines are met and everyone is professional, but they can still be very warm and friendly, being professional. And overall, I really, really enjoyed our communication and appreciated the quality of the finished project.

Vera Wei

Research and Development, Tai Beuty

Cosmetics

Canada

 

Freyr provided excellent support in registering our cosmetic products in the Europe. The team was knowledgeable, efficient, and proactive throughout the process. The communication was clear entirely, which helped us navigate the regulatory requirements without delays. Its delivery aligned perfectly with what was promised up front. No surprises, no delays, just a smooth and transparent service from the beginning to the end. We are quite satisfied with their service.

Poonam Dharman

Packaging and Artwork Director, Lipton Teas and Infusions

Chemicals

Netherlands

 

Working with Freyr has lifted some of the worries and burden of complying with intricate packaging regulations and the ever changing requirements and landscape. We now know that we are in safe hands as we continue working with them. If you are a company who also gets baffled on understanding complicated packaging compliance requirements, then I highly recommend Freyr as a reliable and valuable partner for packaging regulatory projects.

  • Senior Director of Business and Product Development​

    US-based, Leading Innovator Pharmaceuticals Company​

    Medicinal Products

    Regulatory Affairs

    USA

     

    The ANDA receipt has been received! Thank you very much for your hard work, patience, and support for our work over the last couple of months. We are delighted that we were able to meet the timeline and hit an important corporate goal of our young company. ​

    Thank you again, and we look forward to working with your team on the next project!

  • CEO

    US-based, Leading Innovative Pharmaceuticals Company​

    Medicinal Products

    Regulatory Affairs

    USA

     

    Thank you all for the great support!​

  • Assistant Manager​

    US-based, Leading, Complex Generic Pharmaceutical Products Company​

    Medicinal Products

    Regulatory Affairs

    USA

     

    Congratulations!!! ​

    Thanks for your great support for a successful ANDA filing, especially to the publishing team. Heartfully appreciate their last hours of hard work.

  • Director of Regulatory Affairs​

    France-based, Leading Global Supplier of Women Healthcare Products Company​

    Medical Devices

    Publishing and Submission​

    USA

     

    Communication and on the ground knowledge or RA requirements - this has been our experience for India. Quick to response and willing to have calls to explain requirements. Very happy with the RA work conducted in India, would use for other markets. We are satisfied. ​

  • Director

    US-based, Leading Medical Equipment Company​

    Medical Devices

    PAC application ​ submission​

    USA

     

    The team has always been very professional and supportive with our projects and inquiries.  Communication is always timely. Knowledge of regulations, Open Communication, Timely followups with my team and Professionalism. I feel you all work around the clock as you are very responsive on our questions any time of day.  ​

  • Regulatory Affairs Officer​

    US-based, Leading Medical Equipment Company​

    Medical Devices

    Product assessment​ and due diligence​

    USA

     

    Knowledgeable staff, good interpersonal skills and very responsive to requests​

  • 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. ​

  • 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. ​

  • Associate, Clinical & Regulatory Affairs Center

    South Korea-based, Leading Global Chemical Company

    Medical Devices

    Device Registration

    South Korea

     

    Thank you so much, Freyr team, for your support on the way in registering 3 of our medical devices in the Philippines. 

    I hope this achievement will open numerous business opportunities for Freyr and our company to work in synergy.

  • Regulatory Affairs Officer

    UK-based, global Medical Device Manufacturing company

    Medical Devices

    Technical Documentation

    UK

     

    WHOW WHOW WHOW!!!!! YES, YES, YES!!!!! THANK YOU, THANK YOU, THANK YOU!!!!!!

    This call for a celebration. Thank you for your consistency, perseverance, and amazing teamwork at Freyr!!!! THANK YOU.