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Reduce the time and cost of getting new medicines to patients
Prioritizing Patient Safety.
We offer Lean and Agile solutions which will meet your timelines for clinical trials whether you apply in the USA (FDA) and in Europe (EMA).
We can support Sponsors with a wide range of services thanks to our network of clinical experts who can address the different laws across the several European jurisdictions.
Our area of expertise covers:
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Clinical trial's authorisation procedure
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Good Clinical Practice
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Safety Reporting
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Clinical Trial Data Transparency
Our capabilities include
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Quality Assurance & Compliance
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Regulatory
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Pharmacovigilance
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Development
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Medical
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Statistical
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Market Access
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IT & Data Management
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