Development and Co-commercialization

We apply expertise and technology across the medical affairs lifecycle from research and planning to content development, regulatory submissions and health authority query management to ensure seamless compliance in a complex and evolving landscape. Our AI-driven pharmacovigilance platform improves the effectiveness of monitoring, analysis, reporting, and risk mitigation of adverse event signals across the product lifecycle while ensuring continuous regulatory compliance. We improve overall customer engagement with modern medical affairs operations.

We help you scale commercial operations with adaptable, automated modular content, and comprehensive omnichannel campaign management to create outstanding customer experiences. Our proficiency, coupled with technology-driven review and approval operations ensure accurate, impactful, and compliant external communications. With deep data literacy and an analytical knowledge of therapeutics, we maximize the value of your data, translate insights into actions, and drive business outcomes.

Through our partnerships and platforms, we enhance your patient support programs from identification and onboarding to engagement and adherence. Our understanding of patients, payers and HCPs' value perceptions help broaden and deepen market access with data-driven pricing and reimbursement strategies..

We leverage data and analytics through a digital-first approach to enhance your brand planning for maximum impact. With deep insights into healthcare provider behavior, we develop a hyper segmentation model to identify HCPs with the greatest potential to engage digitally and drive prescription behavior. In turn, we use data to create relevant, personalized and scalable content to effectively meet these physicians where they are. We continually monitor content and channel effectiveness to maximize the returns from your marketing investment.

We generate insights from real-world data (RWD) and molecular data to detect gaps in the R&D lifecycle, support biomarker development and improve clinical trial designs. Our targeted digital marketing capabilities enable us to identify patients, conduct efficient primary and secondary screening, and pair them with clinical trial sites, accelerating study startup.

We coordinate contract management, budgeting and payment, data standardization and aggregation, risk-based quality management (RBQM), study-specific portals and patient engagement support. Expert data managers set up and monitor trials ensuring reliable clinical data through protocol-based collection mechanisms.