PubPro
Swap manual tools and clunky legacy platforms with a configurable solution that reduces administrative burden and streamlines compliance.
Approvia IIS
Route research concept submissions from external users through structured, auditable workflows aligned with your unique SOPs.
Approvia Clear
Ensure global compliance and protect brand integrity with a clearance system solution designed for complex, multi-layered review processes.
Approvia MedInfo
Give your medical information team full control and visibility to handle adverse event recordings, HCP dosage questions, and more.
Medical device company scales publication approval output by 4x
Esperion automates publication process with PubPro
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15+ years of experience helping regulated industries streamline complex, high-stakes workflows.
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Proven track record of success supporting large global enterprises and early-stage companies.
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Backed by a dedicated implementation team that knows regulated industries inside and out.
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Flexible platform without the IT overhead thanks to no-code configuration, seamless integrations, and intuitive UX.
FDA Accelerated Approval Guidance: How Automation Ensures Compliance
The FDA’s Accelerated Approval Program was created to fast-track life-saving drugs for serious diseases, allowing life science companies to bring new ...
Webinar Recap: Streamlining Medical Affairs Operations with Technology
In recent years, medical affairs has evolved from a regulatory requirement to a service organization, providing services across functions in ...
Automating Publication Management for Medical Device Companies
The medical device industry is facing mounting pressure to adopt more rigorous publication management practices as regulatory requirements evolve. ...
