When we say quality is the core of everything we do, we have more than words to back this up. The need for compliance with both drug and device standards raises the quality bar for Meridian Medical Technologies, LLC and for every combination product we produce. Most CDMOs supporting combination products excel at some aspect of the development and manufacturing process — but Meridian has more than 60 years of end-to-end service experience to ensure optimal quality at every step.
We work within Quality by Design principles that align with our right-the-first-time mentality. When you choose Meridian, you’re choosing proven industry-leading quality and reliability that bolsters the success of your complex combination product from development through commercialization.
Meridian’s team of innovators excels in competency and expertise with both the medical device and pharmaceutical requirements from the FDA and other international regulators that ensure reliable combination product quality, including full cGMP (Current Good Manufacturing Practices) compliance.
Meridian follows FDA and ICH regulations and guidelines relevant to drug and combination products.
Automation Capabilities
Our optimized automation strategies mean less supply chain risk for you
Measurement Capabilities
We utilize automated measuring equipment to create repeatable, reliable, consistent quality throughout the manufacturing process
X-Ray and CT Scan Capabilities
We implement proactive evaluation time using non-destructive methods to assess products and components
International Quality Control
We also have decades of experience navigating international regulatory and quality standards to facilitate shipping and sales of combination products all over the globe.
From supplier management to operations management through to postmarket, Meridian provides consistent quality throughout the full life cycle of your product.
