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From large multi-national pharmaceutical companies and emerging biotechs to medical device and diagnostics companies, our work is exclusively focused on the life sciences industry.
We use a proven methodology to manage and implement your projects in strict compliance regarding GcP (Good Clinical Practices) from First-in-Human to Phase IV.
Regulatory & Compliance
We are committed to provide you with experts who have a deep knowledge of regulatory requirements on different markets. We are able to support you from regulatory guidelines interpretation to the operational implementation of worldwilde regulatory guidelines.
Safety & Pharmacovigilance
Due to the growing importance of pharmacovigilance, we have established reputable pharmacovigilance groups. We help pharmaceutical companies to process product safety data to ensure compliance with regulations and to establish quality safety databases for effective safety monitoring.
Digitalization, Biometry & Data Management
Elmea offers technological innovations that make drug development more productive, accurate and easier to track.
As a CRO (Contract Research Organization) Elmea delivers deep expertise, objective insights, a tailored approach and unparalleled collaboration to support life sciences leaders.
Elmea consulting practitioners span the entire product development and Lifecycle, adding high-value counsel and recommendations. This participates to optimize clinical developments and brand launches. Together with our clients, Elmea transforms today’s healthcare challenges into tomorrow’s solutions.