Blogs

Submission Suite February 6, 2023
How to Choose the Right eCTD Submissions Vendor: A Comprehensive Guide
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Freyr Submit Track January 13, 2023
eCTD Submissions Planning & Tracking: A Key to Successful Submissions
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Freyr SUBMIT PRO January 4, 2023
Automation: A Helping Hand While Transitioning to eCTD 4.0
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Freyr SUBMIT PRO December 23, 2022
eCTD and CTD Filing Procedures for the US and Canada – Challenges & How to Avoid Them?
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Freyr SUBMIT PRO November 29, 2022
Getting Ready for Adoption of eCTD 4.0
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Freyr SUBMIT PRO November 11, 2022
Streamlining Regulatory Submissions Through Data
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Freyr rDMS November 7, 2022
eDMS - The Driving Force for Successful Regulatory Operations
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Freyr GLASS October 28, 2022
Automating Medical and Scientific Literature Monitoring for Drug Safety (PV)
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Freyr SUBMIT PRO October 13, 2022
eCTD 3.2.2 Vs. eCTD 4.0 - How Significant is the Change?
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Freyr IMPACT September 15, 2022
Automated Regulatory Intelligence (ARI): Keeping you Ahead of the Curve
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Freyr SPAR August 29, 2022
EMA IDMP-SPOR Implementation Guideline v2.1.1 - A Brief Review
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Freyr IMPACT June 28, 2022
Regulatory Intelligence (RI): The Focal Point of Your Business
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