Efficient and responsible product development. Together.

Medical product development, being it medical devices or ATMPs have multiple constituents with numerous challenges and is masked with layers of regulations. From general control of good manufacturing practices and standards to reporting of adverse events, all these factors have major impact on the development cycle of your product.

Together with a number of carefully selected partners, Medace has all the necessary capabilities to support you throughout the entire development process.

Capabilities

Quality is at the heart of everything we do

Assuring a robust and cost-effective manufacturing process

Your experienced partner to navigate the complex regulatory landscape

Because quality management starts early

From facilities to personnel to QMS, Medace focuses on every aspect of bringing your product to clinical operation

From initial concept feasibility to First in Man clinical trials

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