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.
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