Inside the FDA: Pre-Subs, Wellness Devices & Cybersecurity Challenges

Rise of the Regulatory Rebel

FDA 101: Audits, Classification Rules and EU MDR

FDA 101: Understanding the OTHER Regulatory Giant

EU MDR - More then Just Red Tape?

Wait, What - There are Rules?!?!?

QMSR, AI Reviewers and the Value of a Good FDA and Internal Audit

What You Need to Know About FDA Breakthrough Devices

Medical Device Product Development: From Concept to Commercialization

EU Hot Takes: MDD vs MDR featuring Etienne Nichols and Karandeep Singh Badwal

Biocompatibility for MedTech Professionals

CE Certification vs FDA Submission Strategy: Which is Right for You?

ASCA, CLAP, Fraudulent Biocompatibility Data and You

A Conversation with Vistatec's Life Science In-Focus Podcast

eSTAR 5.0 - What You Must Know

The Benefits of 3rd Party FDA Reviewers

eSTAR 5.0 Q+A with Patrick Axtell from the FDA

Fractional or Full Time Quality Support: Which is Right for You?

Medical Devices, Cloud Computing and Cybersecurity with Randy Horton

The Business Benefits of Quality