Transforming scientific advancements into new standards of care.
The ever-evolving landscape of each scientific phase demands precision as you face mounting pressure to optimize returns, secure regulatory approval, and achieve a successful product launch.
We help optimize every step of your pre-commercialization process to accelerate development and inform strategic decision-making. Our expertise lies in translating complex scientific advancements into clear, approachable language that empowers you to set pioneering new standards of care for your patients.
From 2021-2023, we’ve successfully:
Partnered on 328 new molecular entities
Supported products across 14 therapeutic areas
Worked with 66% of the top 20 pharma companies
With deep experience in clinical operations and R&D, our experience covers clinical development operations, trial optimization, data interoperability and standards, safety, pharmacovigilance and more.
We provide comprehensive support for your clinical trials, offering integrated evidence planning, trial design, feasibility analysis, validation, recruitment strategies, trial implementation, retention, and analysis and communication of results.
We support clinical trial communications through earned media, paid social, advocacy relations and internal communications. Our dedicated teams also collaborate with participants, investigators, advocacy groups, and media to promote study recruitment and retention, enhancing community engagement and diversity in participation.
We recruit, train and deploy clinical trial management MSL teams to offer scientific and clinical support to a diverse range of stakeholders. This includes investigators, study co-coordinators, and other healthcare professionals involved in clinical trials.
We help our clients navigate each pivotal moment in their clinical development and commercialization journey so that more people get the treatments they need, faster.
