Reference Data Management Checklist

Checklist

Reference Data Management Checklist

The challenges of effective reference data management are universal.

As you need to manage constantly changing regulatory requirements amid tighter budgets and constrained resources, relying on traditional manual methods of reference data management will no longer suffice.

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Additionally, there is a pressing need for firms to overcome these challenges sooner than later.

As the EMA leads the way in ISO IDMP requirements and SPOR data standards – with other global regulatory agencies soon to follow – firms need to proactively ensure they have the framework in place to not only achieve compliance today but maintain it over time amid ongoing regulatory updates.

Our new checklist outlines what you should prioritize in a reference data management solution to maximize efficiencies, stay compliant with all the latest standards, and harmonize your data ecosystem.

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Mladen Prenc2024-09-10T14:40:40+00:00

ArisGlobal is a pivotal partner in the life sciences industry, specializing in solutions that drive drug development, safety monitoring, and regulatory compliance. We collaborate with more than 500 global life sciences companies, CROs, and government health authorities, including leading biopharmaceutical firms and regulatory bodies such as FDA, Health Canada, and NMPA.
Headquartered in the United States, ArisGlobal has regional offices in Europe, India, Japan and China.

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