10 Small Submissions
No more than 10 Documents per submission
No more than 10 Documents per submission
No more than 75 documents per submission
Open Text Documentum, Veeva Vault, and Master Control and Freyr rDMS
Our customer support covers 3 time zones: America, Europe & Africa and Asia
Experienced publishers who have completed 200,000+ global submissions over the past 12+ years supporting 100s of small-mid Bio Pharma companies and several Top 20 large Bio pharma companies. 24 x 5 global publishing teams across 20 locations.
Someone to assist you in your submissions journey.
Our services and technology team are up to date with any Regulatory market intelligence and the transfer of knowledge reflects on the platform swiftly
If you wish to add more Health Authorities to your bundle, it costs an additional $1450
Freyr SUBMIT PRO focuses on implementing all improved features available within the industry for eCTD compliance. Freyr SUBMIT PRO offers cross-referencing, wherein the applicants can mention the path of the physical files instead of duplicating or cloning the actual eCTD document for eCTD compliance. It helps applicants to link relative objects. Also, the applicants can create references within the eCTD submission, Cross referencing helps to reuse the documents from the current as well as the previous submissions.
Phone: +1 908 483 7958 | Email: hello@freyrdigital.com