Biometrics

IVIDATA Life Sciences can help you design, set up, and operate your databases in compliance with applicable regulations. Our team of data managers is made up of experienced consultants specialising in all phases of studies (phase I – II – III, POC, early and compassionate access, registration, observational, post-MA) and a wide range of therapeutic areas. We guarantee operational excellence in the design and data management of clinical trials.

Data scientists in the field of biometrics play a major role, representing a powerful convergence of technology and biology. Working alongside you, our team applies advanced analytical methods to extract meaningful knowledge from biological and medical data, using tools such as Python, R, GitHub, and Docker. They work on specific disciplines, ranging from data collection and pre-processing to modelling and the development of visualisation solutions, while respecting strict regulations and the IT environment.

Our team of programmers provides full support for all your programming and development needs. Whether in SAS, R, SQL, or Python, we provide technical support and comprehensive documentation. Our experts work to international standards (GxP, CDISC, etc.) in a secure, health data hosting HDS-certified environment, guaranteeing the reliability and confidentiality of your data.

Faced with increasing demands in terms of rigour, quality, relevance, and documentation, our biostatisticians work with you throughout your projects to satisfy your needs. We help you define the appropriate statistical methodology, carry out your analyses (managing subcontractors or teams of programmers), write statistical reports, and promote the results of your studies. Thanks to the expertise and commitment of all our teams, we can bring your projects to a successful conclusion and ensure accurate analyses that comply with the quality standards and regulations in force.

Our pharmaco-epidemiologists ensure the scientific quality and operational follow-up of the studies entrusted to them. Working alongside you, they contribute to updating risk management plans and designing pharmaco-epidemiological studies that will shed light on the situation for decision-makers and help to implement actions aimed at improving the state of health of populations as a result of their exposure to drugs or medical devices.

Our experienced medical writers will help you design and promote your results, in compliance with the applicable regulations and your SOP. They are involved in all types of support, whether methodological, dedicated to the implementation and completion of studies, or to the dissemination of results.

For several years now, the ecosystem of real-life data studies has been constantly evolving. The sources are increasingly diversified, and more and more companies are positioning themselves on the subject, aware of the complementary nature of these studies with clinical trials and of their importance at all stages of the drug development cycle. Our RWE specialists put their expertise at your disposal to ensure that studies are conducted properly while optimising their costs and guaranteeing the reliability of their results, in order to speed up the availability of innovative, safe, and effective medicines for patients.