Post-Marketing Clinical Follow Up (PMCF)

Post marketing surveillance to evaluate safety and identify unknown risks of treatment with medical devices.
Benefits
01

Specialised, strategic consulting

We have expertise in short and long-term safety profiling of products. Our protocols are recommended by regulators.
02

Bespoke solutions

We use primary and secondary data to build prospective and retrospective studies that are tailored to your needs.
03

An established record

We have conducted over 150 safety studies with more than 500K subjects worldwide.
Related solutions
Risk Evaluation and Management Programs
Specialized research and consultancy to manage and prevent the known or potential risks associated with medicine.
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Post-Authorization Safety and Efficacy Studies (PASS/PAES)
Investigating the frequency of a medicine’s known adverse events and benefits in a population of real-life users.
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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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Additional solutions
Pharmacoepidemiology

Also within Health