Medical Device Development and Market Strategy: Europe or US First? Or Both?

Meet Our Speakers:

Matthew Nowland, Vice President, Regulatory Affairs, MedTech, Premier Consulting
Michael Edwards, Senior Director, Regulatory Affairs, MedTech, Premier Consulting

Medical and Regulatory Affairs

FDA’s Final Rule on LDTs and Its Impact on Clinical and Regulatory Professionals

By Charles Chrisawn

April 30, 2024

Consulting

3 Characteristics of a Successful Cell and Gene Therapy Nonclinical Program

By Madelyn Huang

April 24, 2024

Show All

Enhancing Clinical Trial Accessibility – Bringing Oncology Trials to Patients

Listen Now

Medical Device Development and Market Strategy: Europe or US First? Or Both?

Meet Our Speakers:

Recent Posts

Medical and Regulatory Affairs

FDA’s Final Rule on LDTs and Its Impact on Clinical and Regulatory Professionals

Consulting

3 Characteristics of a Successful Cell and Gene Therapy Nonclinical Program

FEATURED PODCAST

PREMIER VOICES #15