Clinical Services

Clinical Services

At Accord Research, we provide a quality standard full range CRO service to our clients. We conduct phase I – IV clinical trials for large pharmaceutical companies as well as small biotechnology companies. A typical project commences with study proposal, feasibility, protocol writing and regulatory submission, continues through to monitoring and project management, concluding   with final statistical analysis and report writing.  We can also assist clients with preparation of all aspects of clinical development programs as well as the preparation of scientific hearings for the US or EU regulatory authorities.

We also offer regulatory assistance and bridging studies for Asian Pacific companies who intend to establish their products in the European and US markets.

Accord Research provides services with a detailed focus on the highest quality and timely delivery of all our clinical studies. 

You can see more details about our services in the left section of this page.

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