Life Sciences: Do Quality, Compliance, and ERP Have to Be in Separate Systems?

ERP, QMS, document management, and electronic signatures are often handled in different systems. This means more integrations to maintain, more manual work, and greater difficulty in ensuring traceability throughout the entire process. But does it have to be that way?

In this webinar, we’ll show you how more quality and compliance processes can be managed in an integrated way within Microsoft Dynamics 365 Finance & Supply Chain Management. In 45 minutes, you’ll see concrete examples of how a more cohesive approach can reduce reliance on separate systems and manual processes while providing better control and traceability.

• A clearer picture of which Quality & Compliance processes can be managed in Dynamics 365.
• Concrete examples of CAPA, nonconformance management, electronic signatures, audit trails, and batch traceability.
• Insights into where you can reduce your reliance on separate systems and integrations.
• A new perspective on how you can simplify your system landscape without compromising quality, compliance, or traceability.

Together with Merit Solutions' products, we’ll show you how control and traceability can become a more integrated part of your business processes in Dynamics 365.

The goal is to give you a concrete picture of what data can actually be collected in Dynamics 365 and the potential this can create for your business.

This webinar is primarily intended for those working in IT, Quality, or QA within the life sciences industry who want to reduce the complexity between business systems, quality processes, and compliance.

It is also relevant for those in Regulatory Affairs, Compliance, Operations, Production, or systems architecture. You do not need to be using Dynamics 365 at this time.