With our unique heritage and expertise in co-development, Ergomed’s focus on excellence in execution, quality with agility, and integrity will support you at every stage in the development of your new medicine.

Our talent management strategy is focused on attracting seasoned professionals who are passionate about research and driven to provide added value with elegant and sophisticated solutions to complex clinical challenges. More than 40% of our employees have earned a Ph.D., MD, or advanced degree qualification.

Leveraging our deep experience and expertise developed through managing complex oncology and rare disease research, our teams partner with clients to evaluate the needs of a project and establish how best to deliver our tailored, best-in-class service.

We have an established global presence of close collaborations with KOLs, investigators, clinicians, and sites throughout the world. Our accumulated experience and connections with sites and KOLs mean we can ensure that all deliverables and milestones are met on time and within budget.

We combine this heritage and global presence with in-depth understanding of new technologies, the ability to flex and be agile, and with our passion, integrity, and transparency to support you on every step of your clinical development journey.

Early-stage development

Our combination of extensive clinical knowledge and wide-ranging clinical experience allows us to support protocol design, development, and execution across a broad range of therapeutic areas.

This winning combination of skills and experience allows us to anticipate factors that could impact your early-stage development and to minimize the risk and costs whilst maximizing signals. Our protocol design and optimization service ensures all aspects of the project are fully covered – from biomarkers and endpoints to the patient population and pathways, and local standards of care – allowing for the efficient management and conduct of early-stage trials.

Late-stage development: Knowledge, network, speed, balance

We leverage our know-how and extensive network of investigators and sites to identify the best locations to conduct your research.

With our in-depth feasibility team and an assessment of the regulatory environment, we can develop protocol-specific plans that ensure the delivery of enrollment milestones.

Our track record of delivering quality data that passes inspection and audit to yield marketing authorizations is a testament to our scientific and patient-centric approach to clinical research.

We offer our clients expertise in:

  • Project management
  • Feasibility assessments
  • Regulatory affairs
  • Site support services
  • Clinical monitoring
  • Patient-centric solutions
  • Physician support
  • Medical monitoring
  • Biometrics
  • Medical writing
  • Quality assurance

Post-approval studies

Our 25+ years of experience in real-world, evidence-based research means we can develop solutions to the most complex challenges, enabling the efficient and fast collection of real-world data across many therapeutic areas.

We support clients to establish credible evidence of real-world value through operational techniques that increasingly embrace advanced technologies. Our RWE services are built to support your post-approval steps and strengthen your market position.

We offer our clients expertise in:

  • PASS, PAES studies
  • Natural history studies
  • Compassionate use programs
  • Registries
  • Outcomes research
  • Epidemiology and risk management