Our complete solutions

Ergomed uses its leading expertise in the co-development of drugs to offer a complete, global Phase I-IV clinical development and trial management service.

Explore Our Process

To navigate, click each section and read more about our services and expertise.

Therapeutic Expertise

Phase I

Phase II

Phase III

Phase IV

Phase I

Our experts in early development offer a combination of extensive knowledge in clinical pharmacology, clinical experience in oncology and rare diseases, excellent partnered phase I units in Europe and North America and collaboration with top investigators

This combination of skill and resources allows us to anticipate factors that could impact your early stage development.

Phase II

Phase II clinical trials are an extremly sensitive part of drug development, proving efficacy of your product

Its managment requires highly experienced people able to identify potential claggenges, mitigate risks, engage top investigators, recruit the right patients and design a trial that will build a sound evaluation of your drug.

Phase III

Late stage clinical trials require a balance of know-how with an extensive network. Your project will need a team that can navigate the challenges involved in recruiting huge patient populations whilst meeting clinical standards and regulatory requirements.

Different time zones, languages, cultures and working environments can all add to the complexities of Phase III trials.

Phase IV

Phase IV solutions ensure that your product's potential is fully recognized, With over 30 years of experience, we have accumulated deep expertise across many therapeutic areas.

Using operational texhniques that increasingly embrace advanced technologies, we can support you to objectively and credibly establish evidence of value in real-world-settings.

Our background in co-development means we understand what it takes to deliver drugs to market quickly and responsibly.
0 offices worldwide
0 countries with active clinical trials
0 EU QPPV projects
0 professionals
0 years' experience
0 oncology studies
0 rare disease studies
0 studies completed
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