We ofer you methodological support and advice to conceive your study, as wel as our expertise in early drug development and our access to related experts.
Thanks to our close monitoring of the evolution of relevant legislation, your study wil comply with the regulatory requirements.
To work with us is to be assured to have a wel-designed study meeting your goals: respect of deadlines, precision and quality of the data colected.
Medical support: methodology advice, medical writing Pharmaceutical services, Regulatory services, Global Project Management, Monitoring, Data management (ORACLE CLINICAL®, eCRF), Statistics (SAS®), Bioanalysis, Central laboratory.
We benefit from our broad experience at each step of a clinical study to provide you with al the services you need:
At Eurofins Optimed, we ensure the smooth and swift progress of your study at every step.
From inclusion to study monitoring, from study document definition to the final clinical report, from first-into-human to proof of concept, we provide ful or à la carte services.
Our aim is to fulfil your expectations, respecting your timelines and adding value through our services.
Complete range of services