The current explosion of novel products, data and ever-changing regulatory requirements across multiple geographies and product categories means that medical device and diagnostics companies need better ways of managing and streamlining regulatory information and submissions. The days of manually handling everything from commitments and correspondence to publishing and submissions are obsolete. Finding and employing a purpose-built Regulatory Information Management (RIM) system that integrates with your other product lifecycle systems is essential to meeting your specific needs. The right MedTech RIM system will enable you to increase regulatory compliance speed, collaboration, efficiency and visibility across your portfolio.
Tune in to our webinar for a panel discussion to understand:
The main changes driving adoption of regulatory technology in MedTech
What the future regulatory landscape for MedTech will look like
The relationship and importance between Regulatory Information Management (RIM), Regulatory Intelligence (RID), and Quality Management (QMS) data and processes
Learn what to look for in a RIM for MedTech solution and how to optimize your regulatory processes. Hear from a leading medical device company on how they solved their key challenges. Ask the experts your important questions.