Innovation in regulatory: The art of the possible

Imagine a global, harmonized database where all information relating to medicinal product can be found. IDMP represents an opportunity to drive cross-functional solutions that bring together people, process, and data, breaking all the traditional silos industry has been struggling with to date.

Through the research conducted by the innovation team at The Dock, and collaboration with our regulatory practice, Accenture has brought together artificial intelligence and the need for regulatory compliance.

VIDEO

Accenture and TOPRA IDMP Readiness Webinar

VIDEO

AI in Regulatory

SLIDESHARE

Enabling IDMP through technology

Featured webinar

Adapting to the future of clinical R&D

Marshalling and acting on clinical trial information across the rapidly evolving trial landscape and ecosystem of study partners requires both an adaptable and scalable technology foundation and new ways of working. Accenture will share best practice on using modern architecture to streamline trial processes, improve collaboration, and comply with fast-changing regulations. Moderated by:

  • Bernard Panes, R&D Innovation Lead, Accenture Life Sciences
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Listen now to our adapting to the future of clinical research and development webinar.

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INTIENT Pharmacovigilance On Demand Webinar

This webinar focuses on the INTIENT Pharmacovigilance Product Suite.

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Patient-centric leadership in cell and gene therapy

Learn how organizations are embracing a new cell and gene therapy (CGT) patient journey to transform the clinical operating model.

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Designing a patient-centered clinical trial

Join us as we hear from patients and an expert panel about the critical importance of focusing on the patient in clinical trial design.

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Redefining regulation through data automation

Accenture’s Kim Brownrigg leads this on-demand webinar, taking a look at how intelligent data automation can help redefine Regulatory.

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Life Sciences
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