Data Migration Services

Trust Freyr for your Regulatory data migration needs, offering tailored solutions that utilize state-of-the-art tools and rigorous validation processes to ensure complete compliance and data integrity throughout the transition.

Data Migration Services - Overview

At Freyr, we understand the critical importance of accurate and compliant data migration in the Regulatory publishing and submission process. Our comprehensive data migration services are designed to ensure a seamless transition of your Regulatory data, including all historic sequences and applications, into a new system or format.

Key Features of Freyr's Data Migration Services:

Historic Sequence Collection: We meticulously gather all historic sequences to ensure no data is left behind during the migration process. Our team ensures that every piece of information is accounted for, from initial applications to the latest updates.

Application and Sequence Tracker Creation: To maintain the integrity of your data, we create detailed applications and sequence trackers. These tools are essential for monitoring the migration progress and ensuring that all sequences are correctly aligned with their respective applications.

Migration Tool Utilization: Leveraging advanced migration tools, we facilitate the efficient transfer of your sequences and applications. Our tools are designed to handle complex data sets, ensuring a smooth migration with minimal disruption to your operations.

Verification and Validation: Post-migration, our team conducts thorough verification and validation of the migrated data. This step is crucial to confirm that the data has been accurately transferred and that it meets all Regulatory requirements.

Cross-Verification of ICH and Regional Metadata: We perform an exhaustive cross-verification of all ICH (International Council for Harmonisation) and regional metadata. This ensures that the migrated data is compliant with both international standards and specific regional Regulatory guidelines.

Data Migration Services

  1. We boast a dedicated team that has completed thousands of data migrations and applications globally
  2. We provide tailored assistance for data migration within a month
  3. Our team is highly adaptable to last-minute changes, ensuring flexibility and responsiveness
Data Migration Services for Regulatory Publishing and Submission
  1. Leveraging our deep expertise in Regulatory standards, we ensure that your migrated data is fully compliant with all relevant regulations
  2. Our rigorous processes guarantee the integrity of your data throughout the migration, ensuring no loss or corruption of information
  3. Utilizing state-of-the-art migration tools and methodologies, we deliver a swift and efficient migration process, saving you both time and resources
  4. Our team of seasoned Regulatory experts provides comprehensive support and guidance throughout the migration process, ensuring a seamless transition for your organization
  5. Recognizing that every organization has unique needs, we tailor our services to meet your specific data migration requirements
Data Migration Services for Regulatory Publishing and Submission

Celebrating Customers Success

 

Medicinal Products

Publishing and Submission

UK

We would like to appreciate Freyr’s quick TAT to push through an urgent submission required by the FDA. Their efficiency, diligence, excellence, sense of urgency, and priority are deeply flexibility.

Please keep up the great work as we have many milestones to achieve over the next year.

Ed Venkat

Global CMC Technical Lead

 

Medicinal Products

Publishing and Submission

UK

I am sure you have heard by now that we have received our first-ever approval from the FDA for our Brands division. This is a major milestone for us as well as for my team here in Reg Ops. I would be remiss if I didn’t point out that we would not have been able to do this without the help of your dedicated team. From the original filing, then the following year of responses, all helped get us to final approval.

Thank you Freyr team for a job well done!

Michael Bellero

Sr. Director, Head of Regulatory Operations

 

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 of Regulatory Affairs​

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