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We have profound knowledge in clinical trials planning, execution and management in full compliance with ICH GCP.

We are committed to the highest quality standards and put particular emphasis on QA/QC processes.

We are ready to comply with sponsor’s requirements and procedures.

We have long-term experience of working as a team, which contributes to our efficient work and excellent coordination.

We are competent in the local pharmaceutical market, regulatory environment, geographical and population opportunities of Russia.

We have established long-term collaboration with Key Opinion Leaders, physicians and academia.

 

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