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Biotech Company US

DocShifter helps large US biotech company streamline submissions by generating 30,000 compliant, submission-ready PDF's every month

Helping solve compliant regulatory content challenges

employees
0
documents / month
0
annual revenue
$ 0 billion

more than

marketed products in the US
0

Challenges with previous rendering solution

One of the largest biotechnology companies in the US has selected DocShifter to speed up and automate submission content preparation.

This company was previously using another software to render all regulatory content; consisting of Word, PDF, Excel, TXT, RTF and image files to compliant PDF documents.

Due to many rendering-related (task failures, content processing problems) and other challenges (costs related to Office & Adobe tools), they made the switch to DocShifter.

The DocShifter impact

14 servers

From 37 conversion servers to 14 DocShifter servers on-premise for the same content.

10x

Faster conversion for regulatory and other corporate content.

3 months

Implemented and validated in 3 months.

Efficiency gains in regulatory through automation

Quality

“During our initial tests, equal or higher quality results compared to previous solution. Higher and more reliable quality results were confirmed.”

Cost

“The overall cost to maintain the legacy solution was very high due to the larger number of servers needed for the load and the multiple additional licensing needed to support those applications (OS, Office, Adobe, etc.).”

Risk

“While testing DocShifter, it was clear that there would be less system downtime and server issues than with legacy solutions. The higher quality output also reduces our risk of non-compliance.”

We use DocShifter to prepare compliant, submission-ready PDF renditions for all regulatory content. The product is reliable, extremely fast and produces output that is compliant with multiple Health Authorities.

Regulatory Information Systems Manager
Large US biotech company