Unified oversight and solid support from a consistent team
We provide seamless consistency and stability across every project, streamlined communication through one central point of contact, and the assurance that your project history and preferred ways of working are always retained, no matter how your internal landscape shifts.
Benefit from portfolio-wide visibility, simplified invoicing, reduced vendor management, and the confidence that continuity, alignment, and proactive support are an integral part of your partnership.
A biotech sponsor was running seven concurrent studies, including five interconnected Phase III trials, while managing evolving requirements and tight timelines. They needed a partner that could provide strategic leadership, portfolio-wide oversight, and specialist expertise to keep studies aligned and progressing efficiently.
Veramed delivered a Project Portfolio FSP model that provided central leadership across the entire program. Through structured governance, proactive risk management, and access to specialist statistical expertise, Veramed helped the sponsor assess the impact of study changes, maintain consistency across studies, and make informed decisions as the program evolved.
Over two years, Veramed supported delivery across all seven studies, including the successful completion of topline and full primary analyses for two Phase III trials running in parallel. The program achieved 100% of agreed KPIs across approximately 80 assessed metrics and maintained a 100% sponsor quality review pass rate, while the partnership expanded beyond the original scope of work.
Tailored data management solutions enabling you to deliver submission-ready data with confidence.
Expert biostatistics support to design better trials, ensure compliance, and produce clear results.
Getting the right evidence, at the right time, in the right format to make the right decisions.
Seamless compliance, efficiency, and innovation through expert governance, advanced automation, real-time visualisation, and AI-powered solutions.
Veramed offers support across all trial phases, including study design, adaptive and Bayesian design, simulations, protocol development, interim analyses, statistical modelling, regulatory submissions, and publication planning.
Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non.
Yes, Veramed has extensive experience in designing and implementing adaptive and Bayesian trials, helping sponsors optimise study efficiency and decision-making through advanced methodologies.
Veramed offers on-demand consultancy services that adapt to your changing needs, whether you require short-term support for study design;ad-hoc analyses or long-term statistical oversight and strategic guidance throughout your trial. Excepteur sint occaecat cupidatat non.
Veramed has extensive experience supporting clinical research in a range of therapeutic areas, with particular expertise in oncology, rare diseases, immunology, cardiovascular and vaccine trials.
Veramed traditionally works with clinical trial data, including complex data, and also has experience working with data from real world (RWE) settings.
