Contributing Writer


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MedTech Strategist, Market Pathways, and the Community Blog are pleased to feature thought leadership contributed by medical device industry executives, regulators, consultants, investors, clinical KOLs, and other experts from the global medtech community.

Articles from Contributing Writer:

Regulatory & Reimbursement

Three Steps to Use Technology to Modernize Clinical Trials

Development in medical device clinical trials has not matched the industry’s rate of product development. Here are several ways companies can accelerate software implementation to make studies more efficient. By Nicole Bongers, Veeva MedTech.

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