Accelerating Regulatory Success with Tailored Solutions **

Certara Regulatory Science provides customized regulatory strategy, document authoring, medical communications, and operations solutions to assure and accelerate the approval of medical innovations. With deep technical and therapeutic expertise across all submission types, Certara's regulatory and medical writers create high-quality documents on time, every time. They also offer expert planning and writing for medical affairs and scientific communications to reach the right audiences. Additionally, their regulatory consulting and operations services streamline electronic submissions and provide visibility throughout the entire process. Certara leverages advanced technologies to enhance speed and efficiency while maintaining an unrivaled commitment to quality and compliance. This unique combination of expertise, technology, and rigorous quality control processes allows Certara to proactively partner with clients to evaluate programs, ensure compliance, and map efficient and effective operational plans to achieve regulatory milestones. With Certara's end-to-end support from R&D through lifecycle management, clients can get it right the first time and avoid costly delays on the path to approval.

With a proven record of success built over decades in the industry, Certara Regulatory Science helps assure and accelerate access to medical innovations worldwide.