Achieve regulatory compliance with exceptional quality standards
Improved medical device design, testing, clinical diagnosis and regulatory science along with ”in-silico” design, a shift toward biologics, and outcomes-based health economics can help accelerate the best products to market, reducing the overall Life Sciences industry attrition rate.
The goal is to create an integrated framework for compliant innovation, embed quality and regulatory best practices early in the development process, and to provide end-to-end product traceability throughout the lifecycle of the product. This process allows for higher quality, compliant products and faster regulatory approvals.
Ensure full regulatory compliance to:
Patients are demanding higher quality and efficacious therapies
An integrated framework for compliant innovation, with embedded quality and regulatory best practices will help meet the demands of both government regulators and patient demands.
The 3DEXPERIENCE® platform is the only solution providing a single environment where manufacturers can work more closely with customers and develop customized solutions at unprecedented speed, efficiency, and cost. Enhanced multi-site collaboration allows them to manage and coordinate facility capacity, operations, inventory and resources in a way that’s profitable and efficient.