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Experts

Sarah Frank

Sarah Frank helps medical device manufacturers overcome complex reprocessing and sterilization challenges, turning regulatory hurdles into pathways to market with expertise that streamlines validation and ensures compliance.

Mark West

Mark West is a recognized expert in the fenestration industry with 15 years of experience in product testing and certification.
Experts

Barry Thomson

Dr Thomson has almost 20 years experience in evaluating polymer performance for the Oil and Gas sector.
Experts

Steve Summerhayes

Steve is a hydrogen expert at ºÚÁϲ»´òìÈ Digital Engineering with extensive experience in advanced hydrogen solutions, spanning design, development, and testing across the aerospace and energy sectors.
Experts

Maciej Jakucki

Maciej Jakucki has performed and managed a wide variety of medical testing projects and programs to meet FDA and CE requirements.
Experts

Tom Elson

Meet our Digital Engineering expert Tom Elson and learn more about his expertise in CFD which enhances our projects with innovative solutions.
Experts

Mark Perkins

Senior Application Chemist with over 22 years of experience in Analytical Chemistry, focusing on the development of SIFT-MS applications.
Experts

Michael Derby

Michael Derby has been in the product development and approvals business for more than 35 years. His present area of expertise is helping manufacturers get radio equipment onto the market.
Experts

Mark Elliott

With almost 30 years of experience, Mark is instantly recognizable in the emissions industry. He brings reliable, honest and insightful decision-making expertise to the table, and demands a culture of safety within the team.
Experts

Nicole Small

Nicole is a highly experienced regulatory professional with a depth and breadth of experience in the safety, performance, and regulation of medical devices – a career spanning over 30 years.

Robert Pieper

Dr. Robert Pieper is an expert in coatings and paints for use with polymeric, rubber, and composite materials and devices.
Resources

Breaking Down the FDA’s Biosimilars Action Plan