When You Need to Design Highly Efficient Studies, It Takes Avania.

Efficiency is essential to medical device development, and a more efficient approach to the development process may often mean the difference between a costly medical device failure and global market success. Consequently, those studies that preemptively consider the overlap between multiple geographies and notified bodies will accelerate timelines and trim budgets without sacrificing data quality.

Where do these overlaps exist? How do you design MedTech studies with these efficiencies in mind? This webinar with Greenlight Guru examines the most efficient means of managing the clinical data necessary for medical device submissions in the U.S. and EU.

Hear from our Senior Director of Strategic Consulting, Mary Kay Sobcinkski, and Senior Medical Writer, Kim van Noort.

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Your product is important, and your trial deserves the team that has what it takes. It takes knowledge. It takes passion. It takes commitment. It Takes Avania.

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