With countless documents required by regulatory agencies for each submission, creating and maintaining them efficiently is difficult.
Templating:
Leverage existing dossiers and documents to enhance productivity.
Sourcing:
Effortlessly trace and monitor the source components of any document.
Reporting:
Seamlessly link your submissions to reports for quicker, more precise reporting.
Tracking:
Monitor the status of submission documents throughout your entire operation.
software solutions can be used with file system or connected to your existing document management system. If you do not have a DMS in place, DOCSmanager might be a perfect fit for you. It has modules specifically developed for the life sciences industries. In addition, we can support you with eCTD Word templates, which make the creation of eCTD documents and dossiers much more efficient. All hubs provide you the greatest flexibility in designing your IT infrastructure on-premise or cloud-based.
Automate your workflows and assign work as needed down your production pipeline. Access the information you need, when you need it across your system. Get supported within your operations from creation to access, review, approval, and publication.
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