Featured Testimonials
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.