51ÁÔÆæ

Susan Schniepp, Distinguished Fellow at 51ÁÔÆæ, discusses the quality metrics journey in determining the suitability of pharmaceutical products. One of the most discussed and debated topics on today’s...

Background A biological drug development company based in Europe came to 51ÁÔÆæ as their facility expansion was under construction. A team of 51ÁÔÆæ experts engaged in guiding this company through...

Whether struggling with a submission strategy and execution or dealing with regulatory compliance, 51ÁÔÆæ stands ready to support your medical device needs. Our consultants have years of experience as regulatory...

The FDA’s regulatory landscape for medical devices is intricate and continually evolving, especially with the advent of innovative technologies like 3D printing and mobile health applications. This white paper from...

In this episode of 51ÁÔÆæ Radio, host Brandon Miller is joined by Jordan Elder, 51ÁÔÆæ'® (51ÁÔÆæ) Regulatory Expert. Kinga Demetriou, an Expert Certifier at BSI, and Nathan Shipley,...

The quest is on for machine learning (ML) to turn raw data into useful medical devices that improve outcomes and reduce burden on the healthcare system. Supporting, and someday emulating,...