Pharma’s experience in honing the management of regulated product data and content presents some useful lessons for medical device suppliers as their own regulatory workloads increase.
A steady progression of health authority (HA) demands in pharma has triggered extensive investment over the last two decades in IT systems and optimised data and content management.
As medical device suppliers adapt to their own rising regulatory commitments, there are some useful best practices emerging from pharma that could serve this sector well as companies strive to maximise their resources.
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