Bob Tilling
VP Global Sales, Kallik
Recent Articles
Disruptive technologies taking the medical device industry by storm
The medical device industry is poised to benefit from greater agility and long-term efficiency savings.
Class II EU MDR regulation – just around the corner
3 key takeaways Class II manufacturers can learn from their Class III counterparts.
EU MDR mandates require more than ad-hoc manual processes
How medical device manufacturers can make labeling operations compliant for European markets.
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