Client Testimonials
  • Director, Regulatory Affairs
    UK-based, Leading Global Medical device company

    Medical Devices

    Device registration

    UK

    “On behalf of Livanova, I would like to thank you, Nisha Vempalle, and her team for the accurate advice and performance, the great commitment, and timely support in successfully completing the MHRA registration process during Y2021 for more than 700 devices. We also appreciate the way you accommodate all Livanova requests in a relationship of mutual trust and respect”.

    We are very satisfied with collaborating with you; looking forward to working with you in Y2022.

  • Manager, Regulatory Affairs
    Spain-based, Leading Medical Devices Company

    Medical Devices

    RAD Safety Report

    Spain

    “Thank you very much for the support. This was a new process for us, and we had plenty of doubts, especially when having strong comments from other internal departments.

    I’m sure Freyr’s team has learned a lot about how to get an accession number. That’s what is really important and gratifying. Thank you again and keep up the excellent work!”

  • Regulatory Specialist
    US-based, Leading IVD Manufacturing Company

    Medical Devices

    MOH account creating support in UAE

    USA

    “Freyr truly exceeded all our expectations and went above and beyond what we asked. Most remarkable is the staff’s quick response time, as they literally seem to be working around the clock. It was an unexpected surprise to have a global partner that was responsive at all hours of the day to our questions and concerns.

    We appreciated that they were always truthful about lead times for queries, submissions, and document reviews. Freyr always delivered when promised, and frankly, the process was easier than we thought. It is very refreshing to feel Freyr’s personal touch, compared to the transactional nature of other consulting partners we have worked with in the past.”

  • Director
    US-based, Leading Precision Medicines Development Company

    Medical Devices

    DMF compilation and Submission

    USA

    I am very satisfied with Freyr's credibility in my interactions. I received good advice that I felt was very above board. Speed of service, responsiveness, attention to my needs, quality of product, and price are all very important, and I felt they were very good in my work with Freyr.

    Thankful to Freyr's responsive team because of which we could comprehend our unusual needs. Rapid responses and the ability to shift direction when needed were very good. I thought the support was very good and met with expectations. In addition, found the price reasonable given the workload.

  • Director, Regulatory Affairs
    US-based, Leading Precision Medicines Development Company

    Medical Devices

    Device registration

    USA

    We have had a good impression of Freyr and feel more than comfortable telling partners that we are engaging with Freyr for our Regulatory needs. The project went very smoothly, and we felt it went along at a reasonable pace. The team was knowledgeable, friendly, and accommodating. Rapid response is appreciated. Keep up the good work.

  • Senior Regulatory Affairs Officer
    UK-based, global Medical Device Manufacturing company

    Medical Devices

    Device registration

    UK

    Thank you for this excellent news, and we would like to express our gratitude to the Freyr team for all the great work and expertise they have brought to the project to make it a success!

  • 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.

  • 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.

  • 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.

  • Trade Dress Manager, Marketing
    Canada-based, Global Generic Pharmaceutical Company

    Pharmaceuticals

    Artwork

    Canada

    Thank you very much for your tremendous efforts to follow up with CCRs and ensure none become overdue. Greatly appreciated!