ABOUT MEDTECH QCS
Meet Barry Camrell
Barry Camrell has spent more than three decades helping medical device companies build stronger quality systems, prepare for audits, solve compliance challenges, and successfully bring products to market.
Throughout his career, he has guided organizations ranging from early-stage companies to established manufacturers through some of the industry's most demanding quality and regulatory requirements.
The Founder has received multiple Quality and World Class Mfg. Awards throughout his career and was the chosen speaker to represent various team achievements in this area of Quality and Lean Six Sigma processes.
More Than 30 Years Helping Medical Device Companies Succeed
WHY MEDTECH QCS
Barry has spent his career working across engineering, quality assurance, quality control, regulatory affairs, design controls, risk management, complaint investigations, and quality management systems.
That broad experience allows him to understand not only regulatory requirements, but also how they affect day-to-day operations, engineering teams, manufacturing processes, and product development.
Experience That Goes Beyond Compliance
30+
Years of Experience in Medical Devices
50+
Products Successfully Brought to Market
25
Years of Successful Audits Supported
Global
Product Launch Experience
Barry’s Area of Expertise
✓ Quality Management Systems (QMS)
✓ FDA Compliance
✓ ISO 13485
✓ MDSAP
✓ Internal Audits
✓ CAPA Management
✓ Quality Assurance
✓ Quality Control
✓ Design Controls
✓ Risk Management
✓ 510(k) Support
✓ Regulatory Affairs
A Personal Note from Barry
Thank you for taking the time to learn more about MEDTECH Quality & Compliance Solutions.
Over the past 30+ years, I've had the privilege of working alongside medical device companies of all sizes, helping them strengthen their quality systems, navigate regulatory requirements, prepare for audits, and successfully bring products to market.
I understand that every organization faces unique challenges. There is no one-size-fits-all solution when it comes to quality management and regulatory compliance. That's why I take the time to understand your current processes, identify potential risks, and develop practical solutions that work for your team—not just on paper, but in day-to-day operations.
Whether you're preparing for an FDA inspection, working toward ISO 13485 or MDSAP certification, navigating a 510(k) submission, strengthening your Quality Management System, or simply looking for experienced guidance during a period of growth or transition, my goal is always the same: to provide practical, experience-driven support that helps your organization move forward with confidence.
I believe the strongest quality systems are built through collaboration, clear communication, and decades of real-world experience. If you're looking for a trusted partner who understands both the engineering and regulatory sides of the medical device industry, I'd welcome the opportunity to learn more about your organization and discuss how I can help.
I look forward to speaking with you.
Click here to schedule a free 30-minute consultation.
Barry Camrell
Founder & Principal Consultant
MEDTECH Quality & Compliance Solutions LLC
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