The regulatory submissions process can span multiple countries, and with people working remotely, using rudimentary tools like Email, Excel and SharePoint, it doesn’t provide the visibility into the latest submission status, thereby limiting the regulatory team’s ability to make effective decisions. This could potentially delay the regulatory submission process.
At Princeton Blue, we recently launched a Regulatory Submission solution that automates the process of creating, approving, and submitting various types of regulatory documents to your health authority. The solution also allows for automating the identification of country-specific documents.
Regulatory submissions are often managed by old legacy systems that don’t talk to each other. We added integrations with existing systems to pull and push data needed for the regulatory submissions.
The ability to modify the workflow and execution parameters such as priorities, owners, due dates, and more, has been important to all our clients, and we incorporated all that into this solution.
Our solution uses workflow automation to monitor the submission process in real-time with in-depth insight into each regulatory submission request. This is crucial to keeping the regulatory operation running smoothly and efficiently. Workflow automation also helps identify potential bottlenecks while ensuring SLA compliance.
In a nutshell, using workflow automation makes regulatory submissions faster, more accurate, and more cost-effective.
I invite you to watch a demo of our Regulatory Submission solution at princetonblue.com to see if workflow automation can help streamline your regulatory submissions.
