Post Marketing Clinical Follow Up

Post Marketing Clinical Follow Up

Post marketing surveillance to evaluate safety and identify unknown risks of treatment with medical devices.
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Featured solutions

Pharmaco-epidemiology

Get help assessing the efficiency and safety of medicines to optimize drug safety.
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Post-Authorization Safety and Efficacy Studies (PASS/PAES)

Investigating the frequency of a medicine’s known adverse events, potential risks, and benefits in a population of real-life users. Robust designs and strategic implementation are key to fulfilling post-authorization commitments.
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Active Surveillance Studies

Evaluate the probability and frequency of adverse events as part of post-marketing risk assessment for medical products.
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Client Results

Safety profiles

We have expertise in short and long-term safety profiling of products. Our protocols are recommended by regulators

Prospect & retrospect

We use primary and secondary data to build prospective and retrospective studies that are tailored to your needs

> 150 studies

We have conducted over 150 safety studies with more than 500K subjects worldwide.