Quality, Regulatory and Safety compliance are the building blocks to ensure medicines and devices are both safe and effective.

The need to comply with ever-shifting global regulatory requirements means an increasing burden on drug and medical device manufacturers. Yet, all too frequently, Quality, Regulatory and Compliance are managed in silos.

Connecting quality management with other enterprise information helps your organization to transform and break down silos, embracing a culture of quality, so vitally important for getting things right first time.

Key takeaways include:

• How a single integrated enterprise platform can help transform your organization into a connected compliance ecosystem

• Learn how to streamline Quality and Regulatory processes, enabling your organization to work more efficiently and effectively, shortening cycle times and costs and reducing compliance risks

• Find out how Regulatory Intelligence, Quality Management, Regulatory Information Management data and processes can work together

Hear from IQVIA Regulatory Intelligence Director Sue Plant and QMS Regulatory and Product Management Director Kari Miller about what to look for in a quality solution and how to optimize your regulatory processes.

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