According to Adlib Software, this new partnership has been formed to facilitate regulatory submissions in the pharmaceutical industry and will see the integration of Good Products’s electronic document management system (eDMS) g-docs with Adlib Software’s Express Server centralized PDF rendering tool.
Adlib Software said that that the collaboration between the two scientific software providers addresses the need from the pharmaceutical industry for streamlined and compliant regulatory document management. Using the new integrated system, pharmaceutical organizations are expected to be able to store, manage and track regulatory documents and create high-quality regulatory submission-ready PDFs with bookmarks and hyperlinks.
g-docs from Good Products allows life sciences organizations to manage their documents including tracking document version history, managing approvals, monitoring and recording changes in an audit log.
Peter Duff, president and CEO of Adlib Software, said: Our partnership with Good Products complements the ability to provide compliant document conversion systems to the pharmaceutical industry. The integration of g-docs and Express Server accelerates regulatory submissions and enables organizations to manage documents in a compliant way across the whole lifecycle, from creation to regulatory submission.
Keith Williams, CEO of Good Products, said: With the increasing standardization of regulatory submissions in an electronic format, and the need to simplify the user experience, both Adlib Software and Good Products recognize the importance of maintaining the consistency and accuracy of electronic documentation from creation to submission. We are now looking to work together to develop further enhancements and functionality, enabling deeper integration of Good Products and Adlib Software solutions.
