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Regulatory Classification Guidance for Saliva Collection Device

12-11-2020 02:06 PM

Case Study

THE PROBLEM: GLOBAL MEDICAL DEVICE COMPANY needed ad-hoc regulatory support in classifying a saliva collection device.  They tapped a consultant they had previously worked with, who already knew their business and market, to provide on-demand support. 

THE SOLUTION: Within hours they were back working with their ad-hoc resource, and within 2 weeks they had the results they were expecting. 

INTERNAL REVIEW:  This project was ideal for the client because they were able to continue to leverage a consultant who was already familiar with their business and products and could hit the ground running in providing regulatory support. 

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