In the highly regulated world of pharmacovigilance, compliance is more than a checkbox—it’s a business imperative. Failing to meet regulatory expectations can lead to significant delays, penalties, and damaged trust. That’s why the tools you use to manage your safety data must be built with compliance at their core.
Progressive ClinConnect doesn’t just support regulatory requirements—it anticipates them. With features designed to ensure audit readiness, data traceability, and alignment with global standards, ClinConnect enables life science organizations to maintain a complete, accurate, and compliant safety database at all times.
Built for Regulatory Excellence
Progressive ClinConnect incorporates a wide array of compliance-centric capabilities that give you full control over your data and peace of mind during inspections or audits:
- Validated Architecture – ClinConnect is fully validated and built for use in GxP environments.
- Full Traceability – Every import, transformation, and decision are logged and documented.
- Audit-Ready by Design – Built-in logging and tracking ensure you’re always prepared for review.
- Submission Data Capture – Automatically populate regulatory reporting fields to minimize manual effort.
- Auto Encoding & Event Assessment – Aligns with MedDRA, WHO Drug, and internal product dictionaries for global compliance.
- Robust Security Controls – Only authorized users can access and operate the platform, reducing exposure to risk.
- Custom Rules for Mapping – Adapt to different agency requirements with flexible transformation logic.
- Selective Approval Workflow – Review and refine data to ensure only accurate, relevant information is processed.
What’s Next?
When compliance is non-negotiable, ClinConnect is the tool you can trust. From the moment data enters the system to the point of regulatory submission, every step is secure, validated, and fully traceable.
Don’t leave your compliance to chance. Contact us today to book a tailored demo and learn how Progressive ClinConnect can help you stay ahead of regulatory demands.