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Post-Marketing Surveillance

We implement safety monitoring systems to address adverse events and ensure ongoing compliance, helping maintain product trust and sustain long-term business growth.

Sustained Sales Growth

We monitor safety, track real-world product performance, and address potential adverse events. This is crucial for maintaining regulatory compliance and ensuring public trust in your product. By offering continuous post-marketing support, we help you optimize sales, maintain regulatory approvals, and enhance your product’s reputation in the industry.

Let Us Support Your Product's Success

SartoMax is committed to accelerating the future of biopharmaceutical development. Contact us to explore more how our CDMO solutions can support your biomanufacturing goals.
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Frequently Asked Questions

Post-market surveillance involves monitoring a product’s safety and performance once launched. It helps identify potential adverse events, ensures continued regulatory compliance, and builds trust with healthcare professionals and patients.
Effective surveillance ensures product safety and maintains public confidence, which is critical for long-term commercial success. Timely responses to safety concerns help protect brand reputation and market share.
Post-market surveillance is required by health authorities such as the UAE Ministry of Health, EMA, and FDA. It includes adverse event reporting, safety updates, and periodic benefit-risk assessments.
We analyze post-marketing feedback and real-world performance data to identify areas for improvement and inform updates to labeling, dosage, or indications.
Our team has expertise in both local (UAE, GCC) and international regulatory frameworks. We tailor our surveillance strategies to meet region-specific requirements while maintaining global standards.

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