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Leveraging Accenture’s global presence and industry engagement, our professionals apply their sophisticated knowledge of regulatory guidelines to help clients stay abreast of the changing environment.
Accenture’s regulatory affairs consultants provide comprehensive regulatory intelligence capabilities that support the development of sound, proactive submission strategies. We assist our clients by identifying potential regulatory hurdles and applying up-to-date intelligence to better facilitate compliance with regional and local requirements and support successful review.
Based on clients’ goals and needs, Accenture subject matter experts and regulatory strategists provide highly-tailored information that focuses on the potential impact of current or anticipated regulatory challenges for clients’ developmental and approved therapies.
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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