Jerry sits on the Qualio quality success team as Manager of Quality Services. He has over 15 years of experience in pharmaceutical, biotechnology and diagnostic laboratory environments. He joined Qualio after 3 years consulting for the CDC.
Articles by Jerry Adatsi
Quality management
8 benefits of a quality management system (QMS) in 2026
Discover the key benefits of a quality management system, its importance, and how it enhances organizational efficiency. Learn more here.
Jerry AdatsiDec 3, 2025
eQMS
Q-Pulse vs. Qualio: a comprehensive guide to eQMS for life science companies
Explore a comprehensive comparison of the Q-Pulse and Qualio eQMS platforms, focusing on features, user feedback, and suitability for different organizational needs.
Jerry AdatsiSep 24, 2024
Quality management
What is a quality management system (QMS)?
What is a quality management system? In a nutshell, it's your company's key to success. Read our breakdown of what a QMS is, and why you need one ASAP!
Jerry AdatsiSep 17, 2024
eQMS
How to Manage the Med Device Software Development Process in Your eQMS
Managing the medical device software development process is a big undertaking.
Jerry AdatsiMay 15, 2024
eQMS
9 core elements of a quality management system [Examples]
Learn everything you need to know about a quality management system (QMS) and how to implement its core elements, so your QMS is compliant and successful.
Jerry AdatsiMar 21, 2024
Pharmaceutical
Top pharma conferences in 2024
Attend the best pharmaceutical conferences in 2024 for pharma industry education and networking opportunities.
Jerry AdatsiDec 1, 2023
GxP
Good distribution practice: understanding GDP compliance
Explore the principles of Good Distribution Practice (GDP) in the pharmaceutical industry, ensuring quality and regulatory compliance in distribution.
Jerry AdatsiNov 1, 2023
FDA
PMA meaning: understanding FDA pre-market approval
Learn what you need to know about the rigorous FDA PMA process including preparing data, documentation and more.
Jerry AdatsiJul 19, 2023
GxP
What you need to know about FDA 21 CFR Part 211
FDA 21 CFR 211 maps out the operational building blocks of cGMP. Understand what you need for compliance, from lab to manufacturing line.
Jerry AdatsiApr 26, 2023
GxP
What you need to know about FDA 21 CFR Part 210
21 CFR 210 compliance is the first step to robust cGMP. Understand what your pharmaceutical or contract manufacturing organization needs in place.
Jerry AdatsiApr 21, 2023
ICH
What is an ICH Q10 pharmaceutical quality system?
What is an ICH Q10 pharmaceutical quality system? It's your company's key to safe, effective and continuously improving products. Learn more with our breakdown guide.
Jerry AdatsiMar 7, 2023
Medical Device Classification
What's the difference between a Class I and Class II medical device?
Learn the difference between a Class I and Class II Medical Device. It's a question that we get all the time and...
Jerry AdatsiJul 28, 2020