With access to vast amounts of data, the risk of false discoveries is high. We help you transform evidence and unlock data insights, turning them into relevant strategies by using advanced methods like AI and machine learning, the application of Bayesian methodology, biomarker statistics, and more. 

We support your clinical trials from start to finish. We help you identify targets, improve reproducibility, and increase efficiency of discovery. This helps to inform better decisions in clinical development. Plus our experts guide you on logistics and storage solutions, tailoring them to fit the needs of your product and your patients. 

Providing global solutions for pharmacovigilance systems and benefit-risk-management services, we support you during clinical trials, clinical document management, literature surveillance, signal management services, PV audits, and more. All with the goal of ensuring compliance with continually evolving regulatory requirements. 

With extensive national health authority experience across the globe, we support you in scientific advice procedures, dossier authoring and submission preparation, and scientific, regulatory and technical writing, from discovery to licensing and post-approval. This includes the European joint clinical assessment (JCA) preparation and readiness.

From clinical to commercial and every point in-between, we can help you accelerate your performance – and your patients' access – to enable healthier futures for all. Our integrated solutions support you wherever you are in the commercialization journey, with global strategic and executional product lifecycle guidance. We ensure a foundation for launch success across global markets, all the way through product distribution and local market delivery. This integrated approach is supported by a suite of enabling technologies that help to automate processes and bridge silos between your internal functions and local affiliates.  

We provide you with strategic consultancy for all quality risk management, change management, and compliance functions in every stage, from development to product withdrawal. From CQV strategy to GxP Technical Consulting Service, we design, develop and implement solutions tailored to your needs. 

Whether designing and executing world-class medical logistics processes or seamlessly connecting our partners to manage and move millions of healthcare products each day, we help your patients access the medications they need, when they need them. Our state-of-the-art storage and distribution facilities, including cold chain solutions, and expertise in distribution and channel strategy improve product performance and support patient access to therapy worldwide. 

Alleviate patient anxiety, identify potential barriers to access, and  increase speed to therapy. We work closely with you to plan, build, and proactively maintain unique copay assistance programs, pair advanced technologies with expert human support, and provide personalized interventions. These not only accelerate access to therapy and improve brand performance, but can have a notable impact on patients’ care experience. 

We can help you better understand each country’s health system to develop effective market access, payer engagement, and commercialization strategies. Generate the evidence needed to demonstrate value, develop your differentiated value story, and communicate it to drive access. Our local knowledge, global reach, and health authority relationships will help you get there. 

Navigate reimbursement issues and other barriers to accelerate speed to therapy with a customized field reimbursement and access support solution. We tailor field support solutions to suit your unique product, providers, and patients. Our consultative approach means you have flexibility to adjust the level of support throughout your product’s entire lifecycle.