Medical device companies today struggle with the continual need for design innovation and faster time-to-market, while under pressure to comply with strict FDA regulations. Compliance with these regulations requires preparing and maintaining accurate sets of extensive documents, which can be a monumental task. Many organizations utilize a paper-based system to meet these requirements, but this type of system can be cumbersome, time consuming, and inefficient. Download the complimentary "FDA Compliance for the Medical Industry Kit" from MatrixOne to discover solutions to these concerns. Information: www.matrixone.com.