FDA Rolls Out New Pilot Program Aimed at Increasing Transparency and Improving Drug Research and Development

What’s the Difference Between Premarket Notification 510(k) and Premarket Approval (PMA)?

Qualio's Quick Guide to FDA Medical Device Classification

9 Ways to Ensure Medical Product Compliance Through Quality

FDA issues draft updated recommendations on submitting a new 510(k) for device modifications

What should I expect when the FDA comes knocking?

Pharmaceutical Testing, Training, Documentation Updates from the FDA

5 Ways that a QMS Improves ISO 9001 Management

Quality and Process are Keys to Successful Life Sciences Product Development

Qualio Among Fastest Growing Irish Companies

FDA Provides Wellness Device Testing Guidelines. What's Your Next Move?

Too Late for a QMS: Theranos' Ignoring FDA Compliance Will Cost it Billions

Case Study: How Qualio helped eHealth Technologies achieve SOC 2 Type II Certification

Life Sciences Conferences for Quality Managers to Attend

How to Rock ISO 13485, Cardiaccs Did It 2x Faster with Qualio

We’re changing our name from ZenDoc to Qualio

If it’s not documented, it didn’t happen

Qualio is the Digital/Online Startup of the Year

Taking Qualio Quality Management Software from a concept to reality

This Will Save Us Years – Lean LaunchPad for Life Sciences

Failure to Comply - Document Control in a Regulated Industry

Reinventing Life Science Startups – Evidence-based Entrepreneurship

Reinventing Life Science Startups – Medical Devices and Digital Health

Reinventing Life Science Startups – Therapeutics and Diagnostics

Qualio secures its 1st US partner