EU Post-Market Surveillance: How Doing More Than Minimum Benefits Medtech

Post-market surveillance requirements apply to all products under the Medical Device Regulation. But it is not just about compliance. Companies would do well to evaluate the additional benefits added PMS efforts can offer them, leading devices expert Bassil Akra explained during a recent interview with Medtech Insight. And he explained how small companies can be equally competent at PMS as large companies.