Driving the next evolution of life sciences regulatory.
The life sciences industry is evolving and advances in technology demand changes in the way Regulatory functions operate. Accenture is leading the next evolution by applying leading edge solutions across the drug and device lifecycle that unify innovative technologies with compliance-focused processes. These solutions include robotic process automation (RPA) and artificial intelligence (AI) as well as optimizing value from data by applying analytics. Accenture is helping life science companies capitalize on Intelligent Automation benefits that go beyond the tangible gains of cost, quality and productivity improvements. To learn more, take a deeper dive in our report: Intelligent Life Sciences: Redefining Regulatory through Intelligent Automation.
Industry shifts and advances in technology demand modifications to the way regulatory responsibilities are performed. Accenture is working with our clients to deliver compliance-focused regulatory outcomes to health authorities across the globe.
Supporting the entire submission process, from IND submissions to gaining global health authorities’ approval to lifecycle management.
Helping to navigate Health Authority guidances to support global agency requirements including scientific, manufacturing, compliance and legal.
Achieving regulatory goals through our StartingPoint Template Suite, implementing RIM strategies or adopting our emerging digital technologies.
Global or regional, therapeutically diverse or indication focused, we help streamline processes and cost by reengineering regulatory businesses.
Helping companies achieve greater speed and efficiency in authoring, reviewing and publishing submission documents. Learn more.
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Life sciences regulatory organizations must find ways to operate more efficiently. How emerging technologies can help.
Accenture’s Clinical Biometrics and Submission Services help a pharmaceutical company speed innovative therapy to patients.