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Accenture’s regulatory affairs team delivers the depth and breadth of capabilities that help global life sciences companies manage the complexities of the regulatory environment.
Accenture’s regulatory affairs professionals serve as trusted advisors to life sciences companies on all aspects of the regulatory affairs strategy. They help reduce cost and increase efficiency, while maintaining quality and compliance throughout the product lifecycle.
Accenture facilitates the adoption of a regulatory model that is proactive and predictable, helping drive strategic innovation and maximizing the ability of sponsor companies to maintain existing product portfolios.
Accenture Accelerated R&D Services delivers digitally enabled technologies and services across the clinical, regulatory and pharmacovigilance functions around the globe. This business service allows pharmaceutical companies to bring drugs to market faster, at less cost and with reduced execution risks.
Accenture Accelerated R&D Services can help our clients:
We work with industry-leading Life Sciences companies in more than 50 countries, as well as more than 125 public health organizations. We have more than 20 years of global delivery experience.
Through a broad array of consulting services for regulatory affairs and operations, Accenture supports all aspects of global submission management. Our service offerings are joined with advanced technology to offer flexible solutions that address functional needs and augment in-house capabilities. Additional services include:
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