The client is a Canada-based fast growing pharmaceutical company, associated with Freyr for Regulatory Publishing and Submissions. To enable their products DIN compliant, they approached Freyr for electronic submissions as per Module 1 DTD version 2.2. The major drawback to kick off the project was that the client had no knowledge on electronic submissions and their requirements.
Download this case to know more on how Freyr educated the client on migration from paper to eCTD format and successfully helped them to continue to be a Lifecycle submission partner.
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