What Makes Sarjen’s RIMS the Smarter Choice?
Now that you’re thinking about switching from spreadsheets, let’s talk about what Sarjen’s RIMS offers — and why it’s built to make regulatory management smarter, faster, and easier for you.
Features That Work for You
- Product Lifecycle Management: Track every stage, from development to market and beyond, in one centralized system.
- Authorization & Approval Management: Accelerate approvals, track statuses, and manage global authorizations seamlessly.
- Variation & Query Tracking: Keep track of regulatory variations and health authority queries without messy spreadsheets.
- Submission Planning: Plan, organize, and monitor submissions across regions — no more last-minute scrambles.
Why Sarjen’s RIMS Stands Out
- Bulk Insert & Update: Upload or modify data in one go — no more manual data dumps.
- Power BI Integration: Turn your regulatory data into powerful dashboards and insights.
- Global Market Coverage: One platform for all regions — track approvals, variations, and submissions globally.
- IDMP-Ready: Stay ahead of evolving compliance standards with an IDMP-compatible system.
If your current processes are slowing you down, it’s time to switch smarter — and Sarjen’s RIMS is built to make that transition smooth, secure, and worth it.
Switch Smarter. Switch to RIMS.
Reach out to us at sarjen@sarjen.com to get started.
Comments are closed.